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

3-Chloropropylamine → N-(3-chloropropyl)-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide

HRID 39575
Notes
Print preview

Reaction equation

HRID 39575 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[CH:18]=[N:17][CH:16]=[CH:15][C:11]=1[C:12]([OH:14])=O.[Cl:19][CH2:20][CH2:21][CH2:22][NH2:23]>>[Cl:19][CH2:20][CH2:21][CH2:22][NH:23][C:12](=[O:14])[C:11]1[CH:15]=[CH:16][N:17]=[CH:18][C:10]=1[NH:9][C:3]1[CH:4]=[CH:5][C:6]([I:8])=[CH:7][C:2]=1[F:1]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 846293-ChloropropylamineHCID 590267913-((2-Fluoro-4-iodophenyl)amino)isonicotinic acid2×

Product 1

HCID 11633443N-(3-chloropropyl)-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide

Procedure

N-(3-chloropropyl)-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide was synthesized according to the procedure for General Method 1, outlined above, starting with 1 mmol of 3-[(2-fluoro-4-iodophenyl)amino]isonicotinic acid (intermediate 1) and 1.3 mmol of 3-chloropropylamine. LC/MS [9.24 min; 434 (M+1)]

Workup

  1. customLC/MS [9.24 min; 434 (M+1)]

Sources & evidence

ORD record
ord-4a6d5745b26947f79e5869e663758dab
Source dataset
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08524911B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes