4-(Trifluoromethoxy)benzylamine → HCID 86695656, compound

HRID 594680Notes

Reaction equation

HRID 594680 reaction equation
[F:1][C:2]([F:13])([F:12])[O:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][NH2:11])=[CH:6][CH:5]=1.[F:14][C:15]1[C:16]([O:24][CH3:25])=[C:17]([C:20]([F:23])=[CH:21][CH:22]=1)[CH:18]=O>>[F:14][C:15]1[C:16]([O:24][CH3:25])=[C:17]([CH:18]2[N:11]([CH2:10][C:7]3[CH:6]=[CH:5][C:4]([O:3][C:2]([F:12])([F:13])[F:1])=[CH:9][CH:8]=3)[C:16](=[O:24])[CH:15]([F:14])[CH2:22]2)[C:20]([F:23])=[CH:21][CH:22]=1

Participants

3

Reactant 2

HCID 5718464-(Trifluoromethoxy)benzylamineHCID 269850393,6-Difluoro-2-methoxybenzaldehyde

Product 1

HCID 86695656HCID 86695656, compound

Procedure

Prepared according to the described general procedures 10A2 (GP10A2), 10B (GP10B), 10F (GP10F), and 10I (GP10I) using commercially available (4-(trifluoromethoxy)phenyl)methanamine and synthesized 3,6-difluoro-2-methoxybenzaldehyde. Subsequent purification by preparative HPLC afforded the target compound. LC-MS (conditions A): tR=0.90 min.; [M+H]+: 419.85 g/mol.

Workup

  1. customPrepared
  2. customSubsequent purification by preparative HPLC
  3. customafforded the target compound

Sources & evidence

ORD record
ord-a968002098d240a395f7758922b1f6cb
Source dataset
uspto-grants-2016_01
Patent number
US09242970B2

Reaction notes

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