Reaction equation
[C:1]1([S:7][C:8]2[N:13]=[C:12]([CH2:14][OH:15])[CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:16][C:17]1[CH:18]=[CH:19][C:20]2[S:24][C:23]([CH:25]([CH:29]([CH3:31])[CH3:30])[C:26](O)=[O:27])=[CH:22][C:21]=2[CH:32]=1>>[Cl:16][C:17]1[CH:18]=[CH:19][C:20]2[S:24][C:23]([CH:25]([CH:29]([CH3:30])[CH3:31])[C:26]([O:15][CH2:14][C:12]3[CH:11]=[CH:10][CH:9]=[C:8]([S:7][C:1]4[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=4)[N:13]=3)=[O:27])=[CH:22][C:21]=2[CH:32]=1Participants
3
Procedure
Using the procedure of Example 10, (6-phenylthio-2-pyridyl)methanol is reacted with 2-(5-chloro-2-benzothienyl)-3-methylbutanoic acid to give (6-phenylthio-2-pyridyl)methyl 2-(5-chloro-2-benzothienyl)-3-methylbutanoate.
Sources & evidence
- ORD record
- ord-732d5490f5024f529786de9404734d2a
- Source dataset
- uspto-grants-1980_09
- Patent number
- US04224330
Linked notes
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