2-Methylnicotinic acid → N-(6-chloro-7-cyclopropylmethoxy-9H-beta-carbolin-8-yl)-2-methyl-nicotinamide

HRID 12196

Reaction equation

HRID 12196 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:12](=[C:13]([NH2:20])[C:14]=1[O:15][CH2:16][CH:17]1[CH2:19][CH2:18]1)[NH:11][C:10]1[CH:9]=[N:8][CH:7]=[CH:6][C:5]2=1.[CH3:21][C:22]1[N:30]=[CH:29][CH:28]=[CH:27][C:23]=1[C:24](O)=[O:25]>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:12](=[C:13]([NH:20][C:24](=[O:25])[C:23]3[CH:27]=[CH:28][CH:29]=[N:30][C:22]=3[CH3:21])[C:14]=1[O:15][CH2:16][CH:17]1[CH2:19][CH2:18]1)[NH:11][C:10]1[CH:9]=[N:8][CH:7]=[CH:6][C:5]2=1

Participants

3

Reactant 2

HCID 6433732-Methylnicotinic acidHCID 671652126-chloro-7-cyclopropylmethoxy-9H-beta-carbolin-8-ylamine

Product 1

HCID 11281226N-(6-chloro-7-cyclopropylmethoxy-9H-beta-carbolin-8-yl)-2-methyl-nicotinamideYield 40%

Procedure

The desired compound was prepared according to Method A from 6-chloro-7-cyclopropylmethoxy-9H-β-carbolin-8-ylamine and 2-methylnicotinic acid in a 40-60% yield.

Sources & evidence

ORD record
ord-970f2d8f6a31410c9eb7931d5d8ac635
Source dataset
uspto-grants-2010_06
Patent number
US07727985B2

Linked notes

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