JPH0564391B2 - - Google Patents

Info

Publication number: JPH0564391B2
Authority: JP; Japan
Prior art keywords: bonds; nodes; reaction; bond; information
Prior art date: 1985-12-28
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Fee Related

Application number

JP60298603A

Other languages

English (en)

Japanese (ja)

Other versions

JPS62157940A (ja

Inventor

Shinsaku Fujita

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Fujifilm Holdings Corp

Original Assignee

Fuji Photo Film Co Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1985-12-28

Filing date

1985-12-28

Publication date

1993-09-14

1985-12-28 Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd

1985-12-28 Priority to JP60298603A priority Critical patent/JPS62157940A/ja

1987-07-13 Publication of JPS62157940A publication Critical patent/JPS62157940A/ja

1993-09-14 Publication of JPH0564391B2 publication Critical patent/JPH0564391B2/ja

Status Granted legal-status Critical Current

Links

238000006243 chemical reaction Methods 0.000 claims description 221
230000007704 transition Effects 0.000 claims description 120
239000000126 substance Substances 0.000 claims description 66
239000007858 starting material Substances 0.000 claims description 46
238000000034 method Methods 0.000 claims description 36
239000000463 material Substances 0.000 claims description 18
238000012545 processing Methods 0.000 claims description 10
230000008569 process Effects 0.000 claims description 6
230000015572 biosynthetic process Effects 0.000 claims description 3
239000000047 product Substances 0.000 description 34
238000004519 manufacturing process Methods 0.000 description 13
150000002500 ions Chemical class 0.000 description 11
150000001875 compounds Chemical class 0.000 description 7
238000010586 diagram Methods 0.000 description 7
230000014509 gene expression Effects 0.000 description 7
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
230000008859 change Effects 0.000 description 5
238000003672 processing method Methods 0.000 description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
230000008901 benefit Effects 0.000 description 4
239000012954 diazonium Substances 0.000 description 4
150000001989 diazonium salts Chemical class 0.000 description 4
238000006460 hydrolysis reaction Methods 0.000 description 4
KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 4
238000003786 synthesis reaction Methods 0.000 description 4
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
239000002253 acid Substances 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
-1 m-nitrophenyl group Chemical group 0.000 description 3
150000002894 organic compounds Chemical class 0.000 description 3
238000011160 research Methods 0.000 description 3
239000011780 sodium chloride Substances 0.000 description 3
229910016467 AlCl 4 Inorganic materials 0.000 description 2
108091023242 Internal transcribed spacer Proteins 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
101100213970 Schizosaccharomyces pombe (strain 972 / ATCC 24843) ypt3 gene Proteins 0.000 description 2
239000003513 alkali Substances 0.000 description 2
238000006757 chemical reactions by type Methods 0.000 description 2
239000002131 composite material Substances 0.000 description 2
238000013461 design Methods 0.000 description 2
150000002466 imines Chemical class 0.000 description 2
230000010365 information processing Effects 0.000 description 2
AMXOYNBUYSYVKV-UHFFFAOYSA-M lithium bromide Chemical compound [Li+].[Br-] AMXOYNBUYSYVKV-UHFFFAOYSA-M 0.000 description 2
230000007246 mechanism Effects 0.000 description 2
125000000896 monocarboxylic acid group Chemical group 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
229940124530 sulfonamide Drugs 0.000 description 2
230000002194 synthesizing effect Effects 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
238000005727 Friedel-Crafts reaction Methods 0.000 description 1
101100109871 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) aro-8 gene Proteins 0.000 description 1
238000009825 accumulation Methods 0.000 description 1
238000005903 acid hydrolysis reaction Methods 0.000 description 1
238000005917 acylation reaction Methods 0.000 description 1
238000005904 alkaline hydrolysis reaction Methods 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000002585 base Substances 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
125000005521 carbonamide group Chemical group 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
CGZZMOTZOONQIA-UHFFFAOYSA-N cycloheptanone Chemical compound O=C1CCCCCC1 CGZZMOTZOONQIA-UHFFFAOYSA-N 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
238000007033 dehydrochlorination reaction Methods 0.000 description 1
238000012938 design process Methods 0.000 description 1
238000011161 development Methods 0.000 description 1
238000007905 drug manufacturing Methods 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000000835 fiber Substances 0.000 description 1
235000019256 formaldehyde Nutrition 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
230000004927 fusion Effects 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000007069 methylation reaction Methods 0.000 description 1
238000000302 molecular modelling Methods 0.000 description 1
238000003541 multi-stage reaction Methods 0.000 description 1
238000005648 named reaction Methods 0.000 description 1
238000010641 nitrile hydrolysis reaction Methods 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
238000006053 organic reaction Methods 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000005215 recombination Methods 0.000 description 1
230000006798 recombination Effects 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
238000012916 structural analysis Methods 0.000 description 1
238000005556 structure-activity relationship Methods 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
238000007039 two-step reaction Methods 0.000 description 1

Landscapes

Information Retrieval, Db Structures And Fs Structures Therefor (AREA)

JP60298603A 1985-12-28 1985-12-28 化学反応情報の記録・検索方法 Granted JPS62157940A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP60298603A JPS62157940A (ja)	1985-12-28	1985-12-28	化学反応情報の記録・検索方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP60298603A JPS62157940A (ja)	1985-12-28	1985-12-28	化学反応情報の記録・検索方法

Publications (2)

Publication Number	Publication Date
JPS62157940A JPS62157940A (ja)	1987-07-13
JPH0564391B2 true JPH0564391B2 (fr)	1993-09-14

Family

ID=17861866

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP60298603A Granted JPS62157940A (ja)	1985-12-28	1985-12-28	化学反応情報の記録・検索方法

Country Status (1)

Country	Link
JP (1)	JPS62157940A (fr)

1985
- 1985-12-28 JP JP60298603A patent/JPS62157940A/ja active Granted

Also Published As

Publication number	Publication date
JPS62157940A (ja)	1987-07-13

Legal Events

Date	Code	Title	Description
2003-09-14	LAPS	Cancellation because of no payment of annual fees

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