4-Thiazoleacetic acid, 2-amino-, ethyl ester → HCID 2814006, 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][N:14]1[CH:18]=[C:17]([S:19](Cl)(=[O:21])=[O:20])[N:16]=[CH:15]1>>[CH3:13][N:14]1[CH:18]=[C:17]([S:19]([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:21])=[O:20])[N:16]=[CH:15]1Participants
3
Procedure
The title compound was prepared from ethyl 2-amino-4-thiazolylacetate and 1-methylimidazole-4-sulfonyl chloride as described in the synthetic METHOD B to give a white solid (3.2 mg) with purity >90%. LCMS (pos) m/z 331.0.
Sources & evidence
- ORD record
- ord-7f11ae5e15b24e839f36e00407b456ee
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07618961B2
Reaction notes
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