Thionyl Chloride → HCID 19860097, compound
Reaction equation
[O:1]=[C:2]([N:9]1[CH2:18][CH2:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:10]1)[CH2:3][N:4]([CH3:8])[CH2:5][CH2:6]O.S(Cl)([Cl:21])=O>C(Cl)(Cl)Cl>[Cl:21][CH2:6][CH2:5][N:4]([CH3:8])[CH2:3][C:2](=[O:1])[N:9]1[CH2:18][CH2:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:10]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The procedure is similar to that described in Example 6b), treating 5.6 g of 2-{N-[2-oxo-2-(1,2,3,4-tetrahydro-2-isoquinolyl) ethyl]methylamino}ethanol with an excess of thionyl chloride in chloroform.
Sources & evidence
- ORD record
- ord-c0b32e1c5dd844828b65a9ad4d959d10
- Source dataset
- uspto-grants-1990_04
- Patent number
- US04914092
Reaction notes
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