4-Thiazoleacetic acid, 2-amino-, ethyl ester → HCID 10133028, compound
Reaction equation
[NH2:1][C:2]1[S:3][CH:4]=[C:5]([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])[N:6]=1.[F:13][C:14]1[CH:15]=[CH:16][C:17]([CH3:24])=[C:18]([S:20](Cl)(=[O:22])=[O:21])[CH:19]=1>>[F:13][C:14]1[CH:15]=[CH:16][C:17]([CH3:24])=[C:18]([S:20]([NH:1][C:2]2[S:3][CH:4]=[C:5]([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])[N:6]=2)(=[O:22])=[O:21])[CH:19]=1Participants
3
Procedure
The title compound was prepared from ethyl 2-amino-4-thiazolylacetate and 5-fluoro-2-methylbenzenesulfonyl chloride as described in the synthetic METHOD B to give a white solid (32.7 mg) with purity >90%. LCMS (pos) m/z 359.2.
Sources & evidence
- ORD record
- ord-65e10228ef834be7a6bc56ff3c922a5d
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07618961B2
Reaction notes
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