2-(Dimethoxymethyl)-1,8-naphthyridine → 7-(Dimethoxymethyl)-1,2,3,4-tetrahydro-1,8-naphthyridine

HRID 1057501노트

반응식

HRID 1057501 반응식
[CH3:1][O:2][CH:3]([O:14][CH3:15])[C:4]1[CH:9]=[CH:8][C:7]2[CH:10]=[CH:11][CH:12]=[N:13][C:6]=2[N:5]=1>CO.[Pd]>[CH3:15][O:14][CH:3]([O:2][CH3:1])[C:4]1[N:5]=[C:6]2[NH:13][CH2:12][CH2:11][CH2:10][C:7]2=[CH:8][CH:9]=1

참가 물질

4

반응물 1

HCID 177501752-(Dimethoxymethyl)-1,8-naphthyridine

생성물 1

HCID 177501767-(Dimethoxymethyl)-1,2,3,4-tetrahydro-1,8-naphthyridine

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

Dimethoxypyridino[3,2-e]pyridin-2-ylmethane was dissolved in methanol (0.5M) followed by addition of 10% Pd/C), and subjected to hydrogenation at ballon pressure. The mixture was filtered through celite and concentrated by rotary evaporation. EI-MS m/z 209 (M+H)+.

후처리

  1. filtrationThe mixture was filtered through celite and
  2. concentrationconcentrated by rotary evaporation

출처 및 근거

ORD 기록
ord-46fec5666b514783adf423d7fff154e8
출처 데이터셋
uspto-grants-2003_02
특허 번호
US06514964B1

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