1-[4-(Bromomethyl)Phenyl]-1H-Pyrazole → HCID 69082568, compound

HRID 594586Notes

Reaction equation

HRID 594586 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH3:10])[C:4]=1[CH:11]1[NH:16][C:15](=[O:17])[CH2:14][CH2:13][CH2:12]1.Br[CH2:19][C:20]1[CH:25]=[CH:24][C:23]([N:26]2[CH:30]=[CH:29][CH:28]=[N:27]2)=[CH:22][CH:21]=1>>[N:26]1([C:23]2[CH:24]=[CH:25][C:20]([CH2:19][N:16]3[CH:11]([C:4]4[C:5]([O:9][CH3:10])=[CH:6][CH:7]=[CH:8][C:3]=4[O:2][CH3:1])[CH2:12][CH2:13][CH2:14][C:15]3=[O:17])=[CH:21][CH:22]=2)[CH:30]=[CH:29][CH:28]=[N:27]1

Participants

3

Reactant 2

HCID 27764791-[4-(Bromomethyl)Phenyl]-1H-PyrazoleHCID 690825266-(2,6-Dimethoxyphenyl)piperidin-2-one

Product 1

HCID 69082568HCID 69082568, compound

Procedure

Prepared according to the described general procedure 4 (GP4) by reaction of 6-(2,6-dimethoxyphenyl)piperidin-2-one with commercially available 1-(4-(bromomethyl)phenyl)-1H-pyrazole. Subsequent purification by preparative HPLC afforded the target compound. LC-MS (conditions E): tR=0.73 min.; [M+H]+: 392.16 g/mol.

Workup

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

Sources & evidence

ORD record
ord-ebc5a1b13cd0404f957b5db3ee45c5b4
Source dataset
uspto-grants-2016_01
Patent number
US09242970B2

Reaction notes

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