Chlorosulfonic acid → HCID 59295966, compound
Reaction equation
[O:1]=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([S:12](O)(=[O:14])=[O:13])[CH:10]=2)[C:5]([C:16]([OH:18])=[O:17])=[CH:4][NH:3]1.[Cl:19]S(O)(=O)=O>>[Cl:19][S:12]([C:9]1[CH:10]=[C:11]2[C:6]([C:5]([C:16]([OH:18])=[O:17])=[CH:4][NH:3][C:2]2=[O:1])=[CH:7][CH:8]=1)(=[O:14])=[O:13]Participants
3
Conditions
- Temperature
- 100 °C
Procedure
1-Oxo-7-sulfo 1,2-dihydroisoquinoline-4-carboxylic acid (5 g) was added to chlorosulphonic acid (25 ml). The mixture was heated at 100° C. for 84 h and then slowly dripped onto ice with sting. The mixture was filtered and the residue was washed with water and ether and dried to yield 7-(chlorosulfonyl)-1-oxo-1,2-dihydroisoquinoline-4-carboxylic acid as a buff solid (7.5 g).
Workup
- filtrationThe mixture was filtered
- washthe residue was washed with water and ether
- customdried
Sources & evidence
- ORD record
- ord-44484a78e69841d9a4053e6babcc5d1b
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07709500B2
Reaction notes
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