Benzo[d]isothiazole-3-carbonyl chloride → HCID 25234270, compound
Reaction equation
[N:1]12[CH2:8][CH2:7][C:4]([CH2:9][NH:10][C:11]([C:13]3[C:21]4[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=4)NC=3)=[O:12])([CH2:5][CH2:6]1)[CH2:3][CH2:2]2.[S:22]1C2C=CC=CC=2C(C(Cl)=O)=[N:23]1>>[N:1]12[CH2:8][CH2:7][C:4]([CH2:9][NH:10][C:11]([C:13]3[C:21]4[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=4[S:22][N:23]=3)=[O:12])([CH2:5][CH2:6]1)[CH2:3][CH2:2]2Participants
3
Procedure
N-(quinuclidin-4-ylmethyl)benzo[d]isothiazole-3-carboxamide was prepared in a similar manner to N-((quinuclidin-4-yl)methyl)-1H-indole-3-carboxamide, substituting benzo[d]isothiazole-3-carbonyl chloride as the electrophile.
Sources & evidence
- ORD record
- ord-6c606ebf8c674f9a9aa509a60e9003f4
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08114891B2
Reaction notes
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