4,5-Dihydro-2-thiazolamine → HCID 178489031, compound

HRID 1595422Notes

Reaction equation

HRID 1595422 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[NH:13][C:12]([C:14]3[CH:19]=[CH:18][CH:17]=[C:16]([N+:20]([O-:22])=[O:21])[CH:15]=3)=[N:11][C:10]=2[C:23](O)=[O:24])=[CH:5][CH:4]=1.S(Cl)(Cl)=O.[NH2:30][C:31]1[S:32][CH2:33][CH2:34][N:35]=1>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[NH:13][C:12]([C:14]3[CH:19]=[CH:18][CH:17]=[C:16]([N+:20]([O-:22])=[O:21])[CH:15]=3)=[N:11][C:10]=2[C:23]([NH:30][C:31]2[S:32][CH2:33][CH2:34][N:35]=2)=[O:24])=[CH:5][CH:4]=1

Participants

4

Reactant 3

HCID 156894,5-Dihydro-2-thiazolamineHCID 24386Thionyl ChlorideHCID 178489035HCID 178489035, compound

Product 1

HCID 178489031HCID 178489031, compound

Procedure

5-(4-Methoxyphenyl)-2-(3-nitrophenyl )imidazole-4-carboxylic acid, 1 M hydrochloric acid—ether solution, thionyl chloride and 2-aminothiazoline are reacted and treated in the same manner as in Example 1 to give 5-(4-methoxyphenyl)-2-(3-nitrophenyl)-N-(2-thiazolinyl)imidazole-4-carboxamide.

Workup

  1. additiontreated in the same manner as in Example 1

Sources & evidence

ORD record
ord-465b6976f27e47a8985d311bb5aad990
Source dataset
uspto-grants-2001_09
Patent number
US06288061B1

Reaction notes

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