Triethylamine → HCID 20527123, compound

HRID 67758Notes

Reaction equation

HRID 67758 reaction equation
Br.[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]=[C:10]2[N:14]([CH3:15])[C:13]([C:16]3[CH:21]=[CH:20][C:19]([Cl:22])=[C:18]([S:23](=[O:28])(=[O:27])[N:24]([CH3:26])[CH3:25])[CH:17]=3)=[CH:12][S:11]2)=[CH:5][C:4]=1C.[CH2:30](N(CC)CC)C>>[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]=[C:10]2[N:14]([CH3:15])[C:13]([C:16]3[CH:21]=[CH:20][C:19]([Cl:22])=[C:18]([S:23](=[O:28])(=[O:27])[N:24]([CH3:25])[CH3:26])[CH:17]=3)=[CH:12][S:11]2)=[C:5]([CH3:30])[CH:4]=1

Participants

3

Reactant 2

HCID 8471TriethylamineHCID 205274672-(4-Chloro-3-methylphenyl-imino)-4-(4-chloro-3-dimethylsulfamoylphenyl)-3-methyl-4-thiazoline hydrobromide

Product 1

HCID 20527123HCID 20527123, compound

Procedure

Obtained by a procedure analogous to that indicated in Example 2 (a), from 2-(4-chloro-3-methylphenyl-imino)-4-(4-chloro-3-dimethylsulfamoylphenyl)-3-methyl-4-thiazoline hydrobromide and triethylamine. Melting point 137°-141° C.

Workup

  1. customObtained by a procedure analogous to

Sources & evidence

ORD record
ord-03792c860cee446bb5c816706cec999b
Source dataset
uspto-grants-1982_08
Patent number
US04346088

Reaction notes

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