(Oxan-4-yl)methanol → Rac-[1-(3,4-dichloro-phenyl)-2-oxo-2-[4-(tetrahydro-pyran-4-ylmethoxy)-phenyl]-ethyl]-carbamic acid tert-butyl ester

HRID 384939Notes

Reaction equation

HRID 384939 reaction equation
[C:1]([O:5][C:6](=[O:26])[NH:7][CH:8]([C:18]1[CH:23]=[CH:22][C:21]([Cl:24])=[C:20]([Cl:25])[CH:19]=1)[C:9]([C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=1)=[O:10])([CH3:4])([CH3:3])[CH3:2].[O:27]1[CH2:32][CH2:31][CH:30]([CH2:33]O)[CH2:29][CH2:28]1>>[C:1]([O:5][C:6](=[O:26])[NH:7][CH:8]([C:18]1[CH:23]=[CH:22][C:21]([Cl:24])=[C:20]([Cl:25])[CH:19]=1)[C:9](=[O:10])[C:11]1[CH:12]=[CH:13][C:14]([O:17][CH2:33][CH:30]2[CH2:31][CH2:32][O:27][CH2:28][CH2:29]2)=[CH:15][CH:16]=1)([CH3:4])([CH3:2])[CH3:3]

Participants

3

Procedure

The title compound was prepared from rac-[1-(3,4-dichloro-phenyl)-2-(4-hydroxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester and tetrahydro-2H-pyran-4-ylmethanol in analogy to Example 9c): MS (ISP): 494.2 and 496.1 (M+H)+.

Sources & evidence

ORD record
ord-e4b479c01986446a924c8a3d2c70f422
Source dataset
uspto-grants-2013_02
Patent number
US08367838B2

Reaction notes

Loading…