Sulfuryl chloride → HCID 68781764, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH2:9][NH:8][CH2:7][CH2:6]2.S(Cl)([Cl:16])(=O)=O>CC(O)=O>[Cl:16][C:4]1[C:3]([O:2][CH3:1])=[CH:12][CH:11]=[C:10]2[C:5]=1[CH2:6][CH2:7][NH:8][CH2:9]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5.0 g (31 mmol) 6-Methoxy-1,2,3,4-tetrahydro-isoquinoline in 30 mL AcOH are cooled to 0° C. and 2.7 mL (34 mmol) sulfuryl chloride are added slowly. The resulting mixture is stirred at r.t. over night. The solvent is removed in vacuo and the residue is treated with toluene/ACN 1:1. The precipitate is filtered off and dried at 40° C. in vacuo.
Workup
- customThe solvent is removed in vacuo
- additionthe residue is treated with toluene/ACN 1:1
- filtrationThe precipitate is filtered off
- customdried at 40° C. in vacuo
Sources & evidence
- ORD record
- ord-8dfae1d5ea7a400ca1f00c1e719773b6
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09340510B2
Reaction notes
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