CN1106797A - 取代的二氨基邻苯二甲酰亚胺及类似物的合成 - Google Patents

取代的二氨基邻苯二甲酰亚胺及类似物的合成 Download PDF

Info

Publication number: CN1106797A
Authority: CN; China
Prior art keywords: group; phenyl; low; alkyl group; amino
Prior art date: 1993-09-21
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.): Pending

Application number

CN 94115325

Other languages

English (en)

Chinese (zh)

Inventor

U·特林克斯

P·特拉克斯勒

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.)

Novartis AG

Original Assignee

Ciba Geigy AG

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.)

1993-09-21

Filing date

1994-09-20

Publication date

1995-08-16

1994-06-02 Priority claimed from GB9411032A external-priority patent/GB9411032D0/en

1994-09-20 Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG

1995-08-16 Publication of CN1106797A publication Critical patent/CN1106797A/zh

Status Pending legal-status Critical Current

Links

230000015572 biosynthetic process Effects 0.000 title description 3
YTJWBAMDRDWGEG-UHFFFAOYSA-N 4,5-diaminoisoindole-1,3-dione Chemical class NC1=CC=C2C(=O)NC(=O)C2=C1N YTJWBAMDRDWGEG-UHFFFAOYSA-N 0.000 title description 2
238000003786 synthesis reaction Methods 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims abstract description 138
238000002360 preparation method Methods 0.000 claims abstract description 26
125000000217 alkyl group Chemical group 0.000 claims description 117
-1 amino, hydroxyl Chemical group 0.000 claims description 77
239000001257 hydrogen Substances 0.000 claims description 64
229910052739 hydrogen Inorganic materials 0.000 claims description 64
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 61
150000003839 salts Chemical class 0.000 claims description 61
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238000000034 method Methods 0.000 claims description 41
229910052736 halogen Inorganic materials 0.000 claims description 37
150000002367 halogens Chemical class 0.000 claims description 37
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 33
125000003118 aryl group Chemical group 0.000 claims description 33
238000006243 chemical reaction Methods 0.000 claims description 33
125000003282 alkyl amino group Chemical group 0.000 claims description 32
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125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 22
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239000000203 mixture Substances 0.000 claims description 19
125000004432 carbon atom Chemical group C* 0.000 claims description 18
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125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 17
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 15
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229910052757 nitrogen Inorganic materials 0.000 claims description 14
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239000002994 raw material Substances 0.000 claims description 13
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230000000694 effects Effects 0.000 claims description 9
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PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 8
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125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims description 7
125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims description 7
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MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 claims description 6
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125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 6
125000001072 heteroaryl group Chemical group 0.000 claims description 5
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125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 4
125000005133 alkynyloxy group Chemical group 0.000 claims description 4
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CN 94115325 1993-09-21 1994-09-20 取代的二氨基邻苯二甲酰亚胺及类似物的合成 Pending CN1106797A (zh)

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US12491593A	1993-09-21	1993-09-21
US124,915		1993-09-21
GB9411032A GB9411032D0 (en)	1994-06-02	1994-06-02	Synthesis of substituted diaminophthalimides and analogues
GB9411032.7		1994-06-02

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CN (1)	CN1106797A (fr)
DK (1)	DK101994A (fr)
HU (1)	HUT70444A (fr)
MA (1)	MA23336A1 (fr)
PL (1)	PL305095A1 (fr)

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN105949091A (zh) *	2016-03-17	2016-09-21	田子馨	一种苯酐尿素制备2-氯磺酰基苯甲酸甲酯的方法

1994
- 1994-09-02 DK DK101994A patent/DK101994A/da not_active Application Discontinuation
- 1994-09-19 PL PL30509594A patent/PL305095A1/xx unknown
- 1994-09-20 HU HU9402710A patent/HUT70444A/hu unknown
- 1994-09-20 CN CN 94115325 patent/CN1106797A/zh active Pending
- 1994-09-21 MA MA23656A patent/MA23336A1/fr unknown

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN105949091A (zh) *	2016-03-17	2016-09-21	田子馨	一种苯酐尿素制备2-氯磺酰基苯甲酸甲酯的方法

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HU9402710D0 (en)	1995-02-28
DK101994A (da)	1995-03-22
MA23336A1 (fr)	1995-04-01
HUT70444A (en)	1995-10-30
PL305095A1 (en)	1995-04-03

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1995-08-16	C06	Publication
1995-08-16	PB01	Publication
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1996-12-04	SE01	Entry into force of request for substantive examination
1999-12-15	C01	Deemed withdrawal of patent application (patent law 1993)

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CN1106797A (zh)	1995-08-16	取代的二氨基邻苯二甲酰亚胺及类似物的合成

CN1106797A - 取代的二氨基邻苯二甲酰亚胺及类似物的合成 - Google Patents

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