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Methylhydrazine → HCID 178481737, 화합물

HRID 1748821
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HRID 1748821 반응식
O=[C:2]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1)[CH2:3][C:4](OCC)=[O:5].[CH3:15][NH:16][NH2:17]>CCO>[CH3:15][N:16]1[C:4]([OH:5])=[CH:3][C:2]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=2)=[N:17]1
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참가 물질

4

반응물 2

HCID 6061MethylhydrazineHCID 2736461Ethyl 3-oxo-3-(pyridin-2-yl)propanoate

생성물 1

HCID 178481737HCID 178481737, 화합물수율 79%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
85 °C

실험 절차

To a solution of ethyl 3-oxo-3-(pyridin-2-yl)propanoate (25.00 g, 129 mmol, Matrix Scientific) in EtOH (60 mL) was added methylhydrazine (6.81 mL, 129 mmol). The mixture was heated at about 85° C. for about 3 h then cooled to rt and concentrated at rt under reduced pressure. The material was triturated with Et2O (40 mL). The solids were collected by filtration then washed with Et2O to give 1-methyl-3-(pyridin-2-yl)-1H-pyrazol-5-ol (17.80 g, 79%). The filtrate was concentrated under reduced pressure then the material was triturated with 1:1 DCM/Et2O. The solids were collected by filtration and washed with Et2O to give a second crop of 1-methyl-3-(pyridin-2-yl)-1H-pyrazol-5-ol (1.20 g, 5%): LC-MS (Table 1, Method g) Rt=1.05 min, m/z 176 (M+H)+; 1H-NMR (DMSO, Bruker 400 MHz) δ 11.05 (s, 1H), 8.50-8.47 (m, 1H), 7.83-7.80 (m, 1H), 7.78-7.69 (m, 1H), 7.24-7.19 (m, 1H), 5.90 (s, 1H), 3.57 (s, 3H).

후처리

  1. temperaturethen cooled to rt
  2. concentrationconcentrated at rt under reduced pressure
  3. customThe material was triturated with Et2O (40 mL)
  4. filtrationThe solids were collected by filtration
  5. washthen washed with Et2O

출처 및 근거

ORD 기록
ord-4274f93feedb4eafb66e06158be77451
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09150592B2

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