HCID 176526843, compound → HCID 178436573, compound

HRID 1730792Notes

Reaction equation

HRID 1730792 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:16][CH2:15][CH2:14][C:13]3[C:12](=[NH:17])[NH:11][C:10](=N)[C:9]2=3)=[CH:4][CH:3]=1.Cl.[CH2:20]([C:22]1[CH:34]=[CH:33][C:25]([NH:26][C:27]2[S:28][CH2:29][C:30](=[NH:32])[N:31]=2)=[CH:24][CH:23]=1)[CH3:21].N=C1C2CCCCC=2C(=N)N1.Cl.N=C1NC(=N)CS1>>[NH:17]=[C:12]1[C:13]2[CH2:14][CH2:15][CH2:16][CH:8]([C:5]3[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=3)[C:9]=2[C:10](=[C:29]2[S:28][C:27]([NH:26][C:25]3[CH:24]=[CH:23][C:22]([CH2:20][CH3:21])=[CH:34][CH:33]=3)=[N:31][C:30]2=[NH:32])[NH:11]1

Participants

5

Procedure

Proceeding in a manner similar to that described above in Example 10, part A but substituting equivalent amounts of 4-(p-chlorophenyl)-4,5,6,7-tetrahydro-1,3-diiminoisoindoline and 2-(p-ethylanilino)-4-imino-2-thiazoline hydrochloride for 4,5,6,7-tetrahydro-1,3-diiminoisoindoline and 2,4-diiminothiazolidine hydrochloride, there is obtained as the product 1-imino-4-(p-chlorophenyl)-4,5,6,7-tetrahydro-3-[2-(p-ethylanilino)-4-imino-2-thiazolin-5-ylidene]isoindoline.

Sources & evidence

ORD record
ord-08443771722b4112ad9f4b9d3b52d680
Source dataset
uspto-grants-1976_11
Patent number
US03993658

Reaction notes

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