SS-3227 → (r)-1-[4-(2,3-Epoxypropoxy)phenyl]-4-(4-trifluoromethoxyphenoxy)piperidine

HRID 1039613Notes

Reaction equation

HRID 1039613 reaction equation
[F:1][C:2]([F:25])([F:24])[O:3][C:4]1[CH:23]=[CH:22][C:7]([O:8][CH:9]2[CH2:14][CH2:13][N:12]([C:15]3[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][CH:16]=3)[CH2:11][CH2:10]2)=[CH:6][CH:5]=1.[CH2:26](OS(C1C=CC([N+]([O-])=O)=CC=1)(=O)=O)[C@@H:27]1[O:29][CH2:28]1>>[O:29]1[CH2:28][C@@H:27]1[CH2:26][O:21][C:18]1[CH:19]=[CH:20][C:15]([N:12]2[CH2:11][CH2:10][CH:9]([O:8][C:7]3[CH:22]=[CH:23][C:4]([O:3][C:2]([F:1])([F:24])[F:25])=[CH:5][CH:6]=3)[CH2:14][CH2:13]2)=[CH:16][CH:17]=1

Participants

3

Procedure

A target compound was manufactured as in Example 1, using 4-[4-(4-trifluoromethoxyphenoxy)piperidin-1-yl]phenol and (R)-glycidylnosylate as starting raw materials.

Sources & evidence

ORD record
ord-cb6794b165e44fa2bf5a6ab7021b3d30
Source dataset
uspto-grants-2013_10
Patent number
US08552188B2

Reaction notes

Loading…