Acetic Anhydride → HCID 71009070, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([S:8]([C:11]2[CH:16]=[CH:15][C:14]3[C:17]4[CH2:22][CH2:21][NH:20][CH2:19][C:18]=4[O:23][C:13]=3[CH:12]=2)(=[O:10])=[O:9])[CH:5]=[CH:6][CH:7]=1.[C:24](OC(=O)C)(=[O:26])[CH3:25]>>[Cl:1][C:2]1[CH:3]=[C:4]([S:8]([C:11]2[CH:16]=[CH:15][C:14]3[C:17]4[CH2:22][CH2:21][N:20]([C:24](=[O:26])[CH3:25])[CH2:19][C:18]=4[O:23][C:13]=3[CH:12]=2)(=[O:9])=[O:10])[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
Prepared as described for Example 612 using 7-[(3-chlorophenyl)sulfonyl]-1,2,3,4-tetrahydro[1]benzofuro[2,3-c]pyridine (Example 344) and acetic anhydride. MS m/z 390 [M+H]+.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-10729dcab80b40928b4b796c9a3aee8a
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765779B2
Reaction notes
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