HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

N-(3-Cyano-4-(ethylsulfonyl)phenyl)acetamide → N-(3-(Aminomethyl)-4-(ethylsulfonyl)phenyl)acetamide

HRID 1667588
Notes
Print preview

Reaction equation

HRID 1667588 reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([NH:14][C:15](=[O:17])[CH3:16])[CH:6]=[CH:7][C:8]=1[S:9]([CH2:12][CH3:13])(=[O:11])=[O:10])#[N:2]>CO.[Ni]>[NH2:2][CH2:1][C:3]1[CH:4]=[C:5]([NH:14][C:15](=[O:17])[CH3:16])[CH:6]=[CH:7][C:8]=1[S:9]([CH2:12][CH3:13])(=[O:11])=[O:10]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 57448183N-(3-Cyano-4-(ethylsulfonyl)phenyl)acetamide

Product 1

HCID 57448184N-(3-(Aminomethyl)-4-(ethylsulfonyl)phenyl)acetamideYield 93.9%

Reagents, catalysts & solvents 2

HCID 935NickelCatalystHCID 887MethanolSolvent

Procedure

To 5C (423 mg, 1.65 mmol) in MeOH (17 mL), Raney Ni (cat) was added. The mixture was stirred under hydrogen (60 psi) for 8 h, then filtered and concentrated to provide 5D (397 mg, 92%). LC-MS: 253.23 (M+H)+.

Workup

  1. filtrationfiltered
  2. concentrationconcentrated

Sources & evidence

ORD record
ord-8077cd3d37524dee9a4260f1c487a12c
Source dataset
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08044242B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes