Acetyl chloride → HCID 18613788, compound
Reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([CH2:6][CH2:7][NH2:8])=[CH:4][CH:3]=1.[C:11](Cl)(=O)[CH3:12]>>[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([CH2:6][CH2:7][NH:8][CH:11]2[CH3:12])=[CH:4][CH:3]=1Participants
3
Procedure
In accordance with the same procedures as in Steps 1, 2, and 3 of Preparation 21, except for using 4-chlorophenethylamine and acetyl chloride, 7-chloro-1-methyl-1,2,3,4-tetrahydroisoquinoline was obtained. In accordance with the same procedures as in Preparation 20, the titled compound was obtained as pale yellow oil. (Yield: 67%) The product was used in the subsequent step without further purification.
Workup
- customIn accordance with the same procedures as in Steps 1, 2, and 3 of Preparation 21
Sources & evidence
- ORD record
- ord-79b7ec8d86c74cffa1053ecf3fd90a07
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07662832B2
Reaction notes
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