4-Thiazoleacetic acid, 2-amino-, ethyl ester → HCID 10271476, 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.[CH3:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:16]=1[S:23](Cl)(=[O:25])=[O:24]>>[CH3:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:16]=1[S:23]([NH: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)(=[O:24])=[O:25]Participants
3
Procedure
The title compound was prepared from ethyl 2-amino-4-thiazolylacetate and 2,5-dimethoxybenzenesulfonyl chloride as described in the synthetic METHOD B to give a white solid (17.0 mg) with purity >80%. LCMS (pos) m/z 387.2.
Sources & evidence
- ORD record
- ord-02e24c49fec04f52be4b222d3c0c032f
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07618961B2
Reaction notes
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