Triethylamine → 2-Chloro-1,3-thiazole-5-sulfonamide
Reaction equation
[Cl:1][C:2]1[S:3][C:4]([S:7](Cl)(=[O:9])=[O:8])=[CH:5][N:6]=1.CC[N:13](CC)CC>>[Cl:1][C:2]1[S:3][C:4]([S:7]([NH2:13])(=[O:9])=[O:8])=[CH:5][N:6]=1Participants
3
Procedure
Prepared by general procedure III from 2-Chloro-thiazole-5-sulfonyl chloride (1.1 g, 5 mmol) and NH40H (0.42 mL, 6 mmol) with Et3N (0.77 mL, 6 mmol to give the title compound as a light-brown solid (610 mg, 61%). MS (ISN) 197[(M−H)−].
Sources & evidence
- ORD record
- ord-bc99af307e574dab9ca36fa1ffcdde08
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07446113B2
Reaction notes
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