2-Piperidino-4-imino-2-thiazoline hydrochloride → HCID 178422518, compound

HRID 1730786Notes

Reaction equation

HRID 1730786 reaction equation
[CH3:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[C:7]2[C:3]=1[C:4](=N)[NH:5][C:6]2=[NH:12].[ClH:14].[NH:15]([C:22]1[S:23][CH2:24][C:25](=[NH:27])[N:26]=1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.N=C1C2C(=CC=CC=2)C(=N)N1.Cl.N1(C2SCC(=N)N=2)CCCCC1>>[ClH:14].[NH:12]=[C:6]1[C:7]2[C:3](=[C:2]([CH3:1])[C:10]([CH3:11])=[CH:9][CH:8]=2)[C:4](=[C:24]2[S:23][C:22]([NH:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[N:26][C:25]2=[NH:27])[NH:5]1

Participants

5

Reactant 4

HCID 162452962-Piperidino-4-imino-2-thiazoline hydrochlorideHCID 178422522HCID 178422522, compoundHCID 178479106HCID 178479106, compoundHCID 178508669HCID 178508669, compound

Product 1

HCID 178422518HCID 178422518, compound

Procedure

When equivalent amounts of 4,5-dimethyl-1,3-diiminoisoindoline and 2-anilino-4-imino-2-thiazoline hydrochloride are substituted for the 1,3-diiminoisoindoline and 2-piperidino-4-imino-2-thiazoline hydrochloride respectively, in the procedure described in Example 9, part B above, there is obtained as the product 1-imino-4,5-dimethyl-3-(2-anilino-4-imino-2-thiazolin-5-ylidene)isoindoline hydrochloride.

Sources & evidence

ORD record
ord-aaee7a7af91e45a58271dc5dfa4e738c
Source dataset
uspto-grants-1976_11
Patent number
US03993658

Reaction notes

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