Methanesulfonyl chloride → HCID 23301388, compound
Reaction equation
[C:1]1([C:7]2[N:8]([NH2:22])[C:9]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[C:10]3[C:15]=2[CH2:14][CH2:13][CH2:12][CH2:11]3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:23][S:24](Cl)(=[O:26])=[O:25]>>[C:16]1([C:9]2[N:8]([N:22]([S:24]([CH3:23])(=[O:26])=[O:25])[S:24]([CH3:23])(=[O:26])=[O:25])[C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)=[C:15]3[C:10]=2[CH2:11][CH2:12][CH2:13][CH2:14]3)[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1Participants
3
Procedure
1,3-Diphenyl-4,5,6,7-tetrahydro-2H-2-isoindolamine (Example 11) is treated with 2 equivalents of methanesulphonyl chloride.
Sources & evidence
- ORD record
- ord-57af81bdc7704ea8bc53c0d53b6c57ad
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06063804
Reaction notes
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