3-(Bromomethyl)-2,6-dichloropyridine → 6-Acetyl-2,9-dichloro-5,6-dihydropyrido [3,2-c][1]benzazocine
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9](=[O:11])[CH3:10])=[C:4]([CH:12]=[CH2:13])[CH:3]=1.Br[CH2:15][C:16]1[C:17](Cl)=[N:18][C:19]([Cl:22])=[CH:20][CH:21]=1.C(N1C2C=CC=CC=2C=CC2N=C(Cl)C(F)=CC=2C1)(=O)C>>[C:9]([N:8]1[C:5]2[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][C:4]=2[CH:12]=[CH:13][C:17]2[N:18]=[C:19]([Cl:22])[CH:20]=[CH:21][C:16]=2[CH2:15]1)(=[O:11])[CH3:10]Participants
4
Procedure
The title compound was prepared from 9B and 13B by a route analogous to that used for the preparation of 1D. HPLC Rt=2.842 min; LCMS Found: (M+H)+=319.
Sources & evidence
- ORD record
- ord-c1fc1939f1f44e33acff79483f87583d
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07378426B2
Reaction notes
Loading…