4-(3-Methoxypyridin-2-yl)butan-1-amine → HCID 20498755, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:4]([CH2:9][CH2:10][CH2:11][CH2:12][NH2:13])=[N:5][CH:6]=[CH:7][CH:8]=1.[N+](N[C:18]1[NH:23][C:22](=[O:24])[C:21]([CH2:25][C:26]2[S:27][C:28]([CH2:31][N:32]([CH2:37][CH2:38][CH2:39][CH3:40])[CH2:33][CH2:34][CH2:35][CH3:36])=[CH:29][CH:30]=2)=[CH:20][N:19]=1)([O-])=O>>[CH3:1][O:2][C:3]1[C:4]([CH2:9][CH2:10][CH2:11][CH2:12][NH:13][C:18]2[NH:23][C:22](=[O:24])[C:21]([CH2:25][C:26]3[S:27][C:28]([CH2:31][N:32]([CH2:33][CH2:34][CH2:35][CH3:36])[CH2:37][CH2:38][CH2:39][CH3:40])=[CH:29][CH:30]=3)=[CH:20][N:19]=2)=[N:5][CH:6]=[CH:7][CH:8]=1Participants
3
Procedure
Reaction of 4-(3-methoxypyridyl)butylamine with 2-nitroamino-5-(5-di-n-butylaminomethyl-2-thienylmethyl)-4-pyrimidone gives 2-[4-(3-methoxypyridyl)butylamino]-5-(5-di-n-butylaminomethyl-2-thienylmethyl)-4-pyrimidone.
Sources & evidence
- ORD record
- ord-7b6fb4cb05124d819e70c3d39f6d7465
- Source dataset
- uspto-grants-1983_06
- Patent number
- US04388317
Reaction notes
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