HCID 176526843, compound → HCID 178489581, compound

HRID 1112544Notes

Reaction equation

HRID 1112544 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:11]2[CH2:19][CH2:18][CH2:17][C:16]3[C:15](=[NH:20])[NH:14][C:13](=N)[C:12]2=3)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[ClH:22].[CH3:23][O:24][C:25]1[CH:37]=[CH:36][CH:35]=[CH:34][C:26]=1[NH:27][C:28]1[S:29][CH2:30][C:31](=[NH:33])[N:32]=1.N=C1C2CCCCC=2C(=N)N1.Cl.N=C1NC(=N)CS1>>[ClH:22].[NH:20]=[C:15]1[C:16]2[CH2:17][CH2:18][CH2:19][CH:11]([C:5]3[CH:6]=[CH:7][C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=3)[C:12]=2[C:13](=[C:30]2[S:29][C:28]([NH:27][C:26]3[CH:34]=[CH:35][CH:36]=[CH:37][C:25]=3[O:24][CH3:23])=[N:32][C:31]2=[NH:33])[NH:14]1

Participants

5

Procedure

When equivalent amounts of 4-(3,4-dimethoxyphenyl)-4,5,6,7-tetrahydro-1,3-diiminoisoindoline and 2-(o-methoxyanilino)-4-imino-2-thiazoline hydrochloride are substituted for the 4,5,6,7-tetrahydro-1,3-diiminoisoindoline and 2,4-diiminothiazolidine hydrochloride respectively, in the procedure described in Example 10, part A above, there is obtained as the product 1-imino-4-(3,4-dimethoxyphenyl)-4,5,6,7-tetrahydro-3-[2-(o-methoxyanilino)-4-imino-2-thiazolin-5-ylidene]isoindoline hydrochloride.

Sources & evidence

ORD record
ord-0c57a9dbfd3a40e48d556f3c3b1ee5c5
Source dataset
uspto-grants-1978_10
Patent number
US04122261

Reaction notes

Loading…