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Ethyl (E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylate → Ethyl 3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)propionate

HRID 2174581
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인쇄 미리보기

반응식

HRID 2174581 반응식
[O:1]=[C:2]1[NH:11][C:10]2[N:9]=[CH:8][C:7](/[CH:12]=[CH:13]/[C:14]([O:16][CH2:17][CH3:18])=[O:15])=[CH:6][C:5]=2[CH2:4][CH2:3]1>CO.[Pd]>[O:1]=[C:2]1[NH:11][C:10]2[N:9]=[CH:8][C:7]([CH2:12][CH2:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])=[CH:6][C:5]=2[CH2:4][CH2:3]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 66905192Ethyl (E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylate

생성물 1

HCID 89602346Ethyl 3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)propionate수율 90.2%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

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온도
27.5 °C

실험 절차

To a stirred solution of 49a (7.7 g, 34.3 mmol) in methanol (150 ml) was added 10% Pd/C (3 g) under nitrogen. The reaction mixture was stirred in presence of H2 gas at 20-35° C. for 16 h. The progress of the reaction was monitored by TLC. After the reaction was completed, the reaction mixture was filtered through celite and concentrated to get the desired compound as a white solid (7 g, 90.2%); 1H NMR (400 MHz, DMSO-d6) δ 10.35 (s, 1H), 7.95 (s, 1H), 7.48 (s, 1H), 4.05 (q, J=7.1 Hz, 2H), 2.83 (t, J=7.6 Hz, 2H), 2.79-2.60 (m, 4H), 2.58-2.55 (m, 2H), 1.16 (m, 3H); MS (ES) m/e 249.1 (M+H)+.

후처리

  1. filtrationthe reaction mixture was filtered through celite
  2. concentrationconcentrated

출처 및 근거

ORD 기록
ord-190efa89e84a4bd39453bc06e14a1bc5
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09062002B2

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