Reaction equation
[CH:1]1([C:6]2[S:7][CH:8]=[C:9]([C:11]([O:13]CC)=[O:12])[N:10]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1.CCC(C1SC=C(C(OCC)=O)N=1)CC>>[CH3:3][CH2:2][CH:1]([C:6]1[S:7][CH:8]=[C:9]([C:11]([OH:13])=[O:12])[N:10]=1)[CH2:5][CH3:4]Participants
3
Procedure
Prepared by the method of Carboxylic Acid 2, step d using ethyl 2-(pentan-3-yl)thiazole-4-carboxylate [Carboxylic Acid 3, step c] (2.8 g) in place of ethyl 2-cyclopentylthiazole-4-carboxylate. Yield 2.3 g.
Sources & evidence
- ORD record
- ord-76b2d6cae4ec44329458240f09fd1ba9
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08476265B2
Linked notes
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