2-Piperidino-4-imino-2-thiazoline hydrochloride → HCID 178446276, compound

HRID 1112537Notes

Reaction equation

HRID 1112537 reaction equation
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]2[C:4]=1[C:5](=N)[NH:6][C:7]2=[NH:14].[ClH:16].[CH3:17][CH:18]([CH2:27][CH3:28])[CH2:19][NH:20][C:21]1[S:22][CH2:23][C:24](=[NH:26])[N:25]=1.N=C1C2C(=CC=CC=2)C(=N)N1.Cl.N1(C2SCC(=N)N=2)CCCCC1>>[ClH:16].[NH:14]=[C:7]1[C:8]2[C:4](=[C:3]([O:2][CH3:1])[CH:11]=[CH:10][C:9]=2[O:12][CH3:13])[C:5](=[C:23]2[S:22][C:21]([NH:20][CH2:19][CH:18]([CH3:17])[CH2:27][CH3:28])=[N:25][C:24]2=[NH:26])[NH:6]1

Participants

5

Reactant 4

HCID 162452962-Piperidino-4-imino-2-thiazoline hydrochlorideHCID 178446279HCID 178446279, compoundHCID 178492519HCID 178492519, compoundHCID 178508669HCID 178508669, compound

Product 1

HCID 178446276HCID 178446276, compound

Procedure

When equivalent amounts of 4,7-dimethoxy-1,3-diiminoisoindoline and 2-(2-methylbutylamino)-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-4,7-dimethoxy-3-[2-(2-methylbutylamino)-4-imino-2-thiazolin-5-ylidene]isoindoline hydrochloride.

Sources & evidence

ORD record
ord-6e41d85448234da38ded7a397e6d9069
Source dataset
uspto-grants-1978_10
Patent number
US04122261

Reaction notes

Loading…