Methylamine → 1-[7-(N-methylcarbamoyl)heptyl]-3-methyl-2-(3-pyridyl)indole
Reaction equation
CO[C:3]([CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][N:12]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[C:14]([CH3:21])=[C:13]1[C:22]1[CH:23]=[N:24][CH:25]=[CH:26][CH:27]=1)=[O:4].[CH3:28][NH2:29]>C(O)CCC>[CH3:28][NH:29][C:3]([CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][N:12]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[C:14]([CH3:21])=[C:13]1[C:22]1[CH:23]=[N:24][CH:25]=[CH:26][CH:27]=1)=[O:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 4 g of 1-(7-methoxycarbonylheptyl)-3-methyl-2-(3-pyridyl)indole in 40 ml of n-butanol is saturated with methylamine and heated on a steam bath in a pressure bottle for 3 days. The reaction mixture is evaporated to dryness and the product is crystallized to yield the 1-[7-(N-methylcarbamoyl)heptyl]-3-methyl-2-(3-pyridyl)indole.
Workup
- temperatureheated on a steam bath in a pressure bottle for 3 days
- customThe reaction mixture is evaporated to dryness
- customthe product is crystallized
Sources & evidence
- ORD record
- ord-0510bc3a236f4f9881b1550649312aac
- Source dataset
- uspto-grants-1984_07
- Patent number
- US04460777
Reaction notes
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