Thiophene-3-boronic acid → Methyl 6-(benzenesulphonylmethyl)-2-methoxy-3-(thien-3-yl)benzoate
Reaction equation
O1[CH:5]=[CH:4][C:3]([C:6]2[C:7]([O:28][CH3:29])=[C:8]([C:14]([CH2:17][S:18]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=3C)(=[O:20])=[O:19])=[CH:15][CH:16]=2)[C:9]([O:11][CH2:12]C)=[O:10])=[CH:2]1.C1([S:36](CC2C(C(OC)=O)=C(OC)C(Br)=CC=2)(=O)=O)C=CC=CC=1.S1C=CC(B(O)O)=C1>>[C:21]1([S:18]([CH2:17][C:14]2[C:8]([C:9]([O:11][CH3:12])=[O:10])=[C:7]([O:28][CH3:29])[C:6]([C:3]3[CH:4]=[CH:5][S:36][CH:2]=3)=[CH:16][CH:15]=2)(=[O:20])=[O:19])[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1Participants
4
Procedure
Prepared by proceeding in a similar manner to Intermediate 28, starting from methyl 6-(benzenesulphonylmethyl)-3-bromo-2-methoxybenzoate (Intermediate 65) and thiophene-3-boronic acid.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-6385f31c88654115b8a2cf17e9f3f0fb
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09067905B2
Reaction notes
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