4-Toluenesulfonyl chloride → HCID 86738753, compound
Reaction equation
[OH:1][CH2:2][C:3]1[N:4]=[C:5]2[CH:11]=[CH:10][C:9]3=[N:12][S:13][CH:14]=[CH:15][C:8]3=[C:6]2[N:7]=1.[C:16]1([CH3:26])[CH:21]=[CH:20][C:19]([S:22](Cl)(=[O:24])=[O:23])=[CH:18][CH:17]=1>>[C:16]1([CH3:26])[CH:21]=[CH:20][C:19]([S:22]([O:1][CH2:2][C:3]2[N:4]=[C:5]3[CH:11]=[CH:10][C:9]4=[N:12][S:13][CH:14]=[CH:15][C:8]4=[C:6]3[N:7]=2)(=[O:24])=[O:23])=[CH:18][CH:17]=1Participants
3
Procedure
2-Hydroxymethyl-thiazinobenzimidazole derivative (Ia) is reacted with p-toluenesulfonyl chloride to produce 2-p-toluenesulfonyloxymethyl-thiazinobenzimidazole derivative (Ib).
Sources & evidence
- ORD record
- ord-7e8b115014cf40f9be8b51e8d26a4e63
- Source dataset
- uspto-grants-1984_05
- Patent number
- US04450109
Reaction notes
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