Ethyl 4-(pyridin-2-ylamino)piperidine-1-carboxylate → N-(Piperidin-4-yl)pyridin-2-amine

HRID 1245449ノート

反応式

HRID 1245449 の反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[NH:7][CH:8]1[CH2:13][CH2:12][N:11](C(OCC)=O)[CH2:10][CH2:9]1>Br>[NH:11]1[CH2:12][CH2:13][CH:8]([NH:7][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=2)[CH2:9][CH2:10]1

参加物

3

実験手順

6 g of ethyl 4-(pyridin-2-ylamino)piperidine-1-carboxylate (23a) were refluxed in 30 ml of 47% HBr for 6 h. Evaporation of the mixture, trituration of the resulting crude product with ethyl acetate/CH3OH (9:1) and renewed drying afforded 7.1 g of white solid; ESI-MS [M+H+]=178.15.

後処理

  1. customEvaporation of the mixture, trituration of the resulting crude product with ethyl acetate/CH3OH (9:1)
  2. customrenewed drying

出典と根拠

ORDレコード
ord-a7ad09585266425da852695aa3693fbe
出典データセット
uspto-grants-2006_10
特許番号
US07125883B1

反応ノート

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