2-Piperidino-4-imino-2-thiazoline hydrochloride → HCID 178423616, compound

HRID 1730793Notes

Reaction equation

HRID 1730793 reaction equation
[CH3:1][C:2]1[C:10]([CH3:11])=[CH:9][C:8]([CH3:12])=[C:7]2[C:3]=1[C:4](=N)[NH:5][C:6]2=[NH:13].Cl.[Cl:16][C:17]1[CH:29]=[CH:28][C:20]([NH:21][C:22]2[S:23][CH2:24][C:25](=[NH:27])[N:26]=2)=[CH:19][CH:18]=1.N=C1C2C(=CC=CC=2)C(=N)N1.Cl.N1(C2SCC(=N)N=2)CCCCC1>>[ClH:16].[NH:13]=[C:6]1[C:7]2[C:3](=[C:2]([CH3:1])[C:10]([CH3:11])=[CH:9][C:8]=2[CH3:12])[C:4](=[C:24]2[S:23][C:22]([NH:21][C:20]3[CH:19]=[CH:18][C:17]([Cl:16])=[CH:29][CH:28]=3)=[N:26][C:25]2=[NH:27])[NH:5]1

Participants

5

Reactant 4

HCID 162452962-Piperidino-4-imino-2-thiazoline hydrochlorideHCID 178423617HCID 178423617, compoundHCID 178479107HCID 178479107, compoundHCID 178508669HCID 178508669, compound

Product 1

HCID 178423616HCID 178423616, compound

Procedure

Employing a procedure similar to that described in Example 9, part B above, but substituting equivalent amounts of 4,5,7-trimethyl-1,3-diiminoisoindoline and 2-(p-chloroanilino)-4-imino-2-thiazoline hydrochloride for 1,3-diiminoisoindoline and 2-piperidino-4-imino-2-thiazoline hydrochloride respectively, there is obtained as the product 1-imino-4,5,7-trimethyl-3-[2-(p-chloroanilino)-4-imino-2-thiazolin-5-ylidene]isoindoline hydrochloride.

Sources & evidence

ORD record
ord-5bc4befca42e42a086c954f625438867
Source dataset
uspto-grants-1976_11
Patent number
US03993658

Reaction notes

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