3-(Bromomethyl)-2,6-dichloropyridine → 6-Acetyl-2-chloro-5,6-dihydropyrido[3,2-c][1]benzazocine
Reaction equation
BrCC1C(Cl)=NC(Cl)=CC=1.[C:11]([N:14]1[C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=2[CH:19]=[CH:18][C:17]2[N:26]=[C:27]([Cl:31])[C:28](F)=[CH:29][C:16]=2[CH2:15]1)(=[O:13])[CH3:12]>>[C:11]([N:14]1[C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=2[CH:19]=[CH:18][C:17]2[N:26]=[C:27]([Cl:31])[CH:28]=[CH:29][C:16]=2[CH2:15]1)(=[O:13])[CH3:12]Participants
3
Procedure
Compound 13C was prepared from bb and 13B by a route analogous to that used for the preparation of 1D. HPLC Rt=2.493 min; LCMS Found: (M+H)+=285.
Sources & evidence
- ORD record
- ord-2019b49b2cda4e10ac154d57f8a64515
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07378426B2
Reaction notes
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