Benzenesulfonyl chloride → Methyl 2-benzenesulphonylamino-5-ethyl-4-methylthiophene-3-carboxylate
Reaction equation
[C:1]1([S:7]([NH:10][C:11]2[S:15][C:14]3[CH2:16][CH2:17]C[CH2:19][C:13]=3[C:12]=2[C:20]([O:22][CH2:23]C)=[O:21])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.NC1SC(CC)=C(C)C=1C(OC)=O.C1(S(Cl)(=O)=O)C=CC=CC=1>>[C:1]1([S:7]([NH:10][C:11]2[S:15][C:14]([CH2:16][CH3:17])=[C:13]([CH3:19])[C:12]=2[C:20]([O:22][CH3:23])=[O:21])(=[O:8])=[O:9])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
4
Procedure
Prepared by proceeding in a similar manner to Intermediate 1, starting from methyl 2-amino-5-ethyl-4-methylthiophene-3-carboxylate and benzenesulphonyl chloride.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-3e6f67c0c939441b9be17c6269b01a61
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09221787B2
Reaction notes
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