4-(Chloromethyl)-1,3-thiazole hydrochloride → HCID 58951473, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:18])[CH2:5][C:6]1[N:7]=[C:8]([C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=2)[O:9][CH:10]=1)[CH3:2].Cl.Cl[CH2:21][C:22]1[N:23]=[CH:24][S:25][CH:26]=1>>[CH2:1]([O:3][C:4](=[O:18])[CH2:5][C:6]1[N:7]=[C:8]([C:11]2[CH:16]=[CH:15][C:14]([O:17][CH2:21][C:22]3[N:23]=[CH:24][S:25][CH:26]=3)=[CH:13][CH:12]=2)[O:9][CH:10]=1)[CH3:2]Participants
3
Procedure
The title compound is prepared in a manner substantially similar to Intermediate 16 from [2-(4-Hydroxy-phenyl)-oxazol-4-yl]-acetic acid ethyl ester (See Intermediate 64) and 4-(chloromethyl)thiazole hydrochloride except KI (2 eq.) is also added. MS (m/e): 345.2 (M+1)
Workup
- additionis also added
Sources & evidence
- ORD record
- ord-0387f3a9a6244a3c8f7f0238d5071a52
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07666871B2
Reaction notes
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