4-(Propan-2-yl)-1,3-thiazole-2-carbonyl chloride → 4-Cyclopropyl-thiazole-2-carbonyl chloride
Reaction equation
C1(C2N=C(C([O-])=O)SC=2)CC1.[Li+].[CH:13]([C:16]1[N:17]=[C:18]([C:21]([Cl:23])=[O:22])[S:19][CH:20]=1)([CH3:15])[CH3:14]>>[CH:13]1([C:16]2[N:17]=[C:18]([C:21]([Cl:23])=[O:22])[S:19][CH:20]=2)[CH2:15][CH2:14]1Participants
3
Procedure
Compound 267a was synthesized from compound 266a (3 g, 1 eq.) as a brown solid in quantitative yield, following the procedure as described for compound 214. MS (ESI, EI+): m/z=170 (MH+).
Sources & evidence
- ORD record
- ord-23da4ab334aa4f95a30c6ca2c5faed6f
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08377962B2
Reaction notes
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