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6-Chloronicotinic acid → 6-Chloro-N-[3-(1H-imidazol-1-yl)-2-methylpropyl]-3-pyridinecarboxamide

HRID 1583992
Notes
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Reaction equation

HRID 1583992 reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=O)=[CH:4][N:3]=1.[N:11]1([CH2:16][CH:17]([CH3:20])[CH2:18][NH2:19])[CH:15]=[CH:14][N:13]=[CH:12]1>>[Cl:1][C:2]1[N:3]=[CH:4][C:5]([C:6]([NH:19][CH2:18][CH:17]([CH3:20])[CH2:16][N:11]2[CH:15]=[CH:14][N:13]=[CH:12]2)=[O:8])=[CH:9][CH:10]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 792226-Chloronicotinic acidHCID 139528593-(1H-Imidazol-1-yl)-2-methylpropan-1-amine

Product 1

HCID 202575786-Chloro-N-[3-(1H-imidazol-1-yl)-2-methylpropyl]-3-pyridinecarboxamide

Procedure

When 6-chloronicotinic acid was reacted with 3-(1H-imidazol-1-yl)-2-methylpropanamine by the procedure of Example 20, the compound of the Example was obtained, mp 102°-104° C.

Sources & evidence

ORD record
ord-2f00c09a639d4026926c57303137cb5e
Source dataset
uspto-grants-1985_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04555519

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes