반응 #1005247

ord-33b53f02418b48518ef71bac0104e40a

반응 방정식

Cc1ccc(C(O)CC(C)N)cn1
1-(2-Methyl-5-pyridyl)-3-amino-n-butanol
N
ammonia
[Br-].[NH4+]
ammonium bromide
N
ammonia
O=B[O-].[Na+]
sodium boranate
CC(=O)CC(=O)c1ccc(C)nc1
(6-methyl-nicotinoyl)-acetone
CC(N)=CC(=O)c1ccc(C)nc1
1-(2-methyl-5-pyridyl)-3-amino-but-2-en-1-one

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타is obtained
  2. 2
    온도heated at 50° for 15 hours

실험 절차

1-(2-Methyl-5-pyridyl)-3-amino-n-butanol can be used as the starting material, is obtained as follows: 20.0 g of (6-methyl-nicotinoyl)-acetone, 200 ml of ethanol and 0.5 g of ammonium bromide are saturated with ammonia at 50° and heated at 50° for 15 hours whilst continuing to introduce ammonia. 8.5 g of sodium boranate are introduced in portions over the course of 1 hour into the solution, obtained above, of 1-(2-methyl-5-pyridyl)-3-amino-but-2-en-1-one of the formula ##EQU46## and the mixture is stirred for 7 hours at 70° . The solvent is distilled off in vacuo and the residue is taken up in 20% strength aqueous potassium hydroxide solution and pentanol-1. After working up in the usual manner, 19.2 g of crude 1-(2-methyl-5-pyridyl)-3-amino-n-butanol of the formula ##EQU47## are obtained from the pentanol solution as an oil which can be purified further by column chromatography.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US03969363uspto-grants-1976_07