Hydrochloric Acid → HCID 22961899, compound
Reaction equation
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([O:8][CH2:9][C@H:10]2[CH2:13][CH2:12][N:11]2[CH3:14])=[CH:4][C:3]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.Cl.CO>CCOCC>[ClH:1].[Cl:1][C:2]1[N:7]=[CH:6][C:5]([O:8][CH2:9][C@H:10]2[CH2:13][CH2:12][N:11]2[CH3:14])=[CH:4][C:3]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 6-chloro-3-(1-methyl-2-(R)-azetidinylmethoxy)-5-phenylpyridine in Et2O was added hydrogen chloride (1.0 M in Et2O) carefully to afford the tittle compound: mp 173-175° C.; 1H NMR (D2O) δ 2.60-2.78 (m, 3H), 3.00 (s, 3H), 4.02 (m, 1H), 4.25 (m, 1H), 4.60-4.78 (m, 2H), 7.56-7.60 (m, 6H), 8.18 (d, 1H, J=2.0 Hz); MS (CI/NH3) m/z 289 (M+H)+. Anal. Calcd for C16H17ClN2O.1.1 HCl: C, 58.43; H, 5.55; N, 8.52. Found: C, 58.37; H, 5.56; N, 8.43. [α]D23 +40.37 (c 0.27, MeOH).
Workup
- customto afford the tittle compound
Sources & evidence
- ORD record
- ord-017ff48a79ee4bb2a8b5e3da68a6a693
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06437138B1
Reaction notes
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