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4-Fluorobenzyl chloride → 3-Cyano-1-(4-fluoro-benzyl)-6-hydroxy-7-oxo-1,7-dihydro-pyrazolo[1,5-a]pyrimidine-5-carboxylic acid 4-fluoro-benzylamide

HRID 536119
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인쇄 미리보기

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HRID 536119 반응식
[H-].[Na+].[F:3][C:4]1[CH:11]=[CH:10][C:7]([CH2:8]N)=[CH:6][CH:5]=1.[F:12][C:13]1[CH:35]=[CH:34][C:16]([CH2:17][NH:18][C:19]([C:21]2[N:22]=[C:23]3[C:31]([C:32]#[N:33])=[CH:30][NH:29][N:24]3[C:25](=[O:28])[C:26]=2[OH:27])=[O:20])=[CH:15][CH:14]=1.FC1C=CC(CCl)=CC=1>CN(C=O)C>[F:12][C:13]1[CH:14]=[CH:15][C:16]([CH2:17][NH:18][C:19]([C:21]2[N:22]=[C:23]3[C:31]([C:32]#[N:33])=[CH:30][N:29]([CH2:8][C:7]4[CH:10]=[CH:11][C:4]([F:3])=[CH:5][CH:6]=4)[N:24]3[C:25](=[O:28])[C:26]=2[OH:27])=[O:20])=[CH:34][CH:35]=1
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참가 물질

5

반응물 3

HCID 96024-Fluorobenzyl chlorideHCID 24758Sodium hydrideHCID 866430543-cyano-N-[(4-fluorophenyl)methyl]-6-hydroxy-7-oxo-1H-pyrazolo[1,5-a]pyrimidine-5-carboxamide;(4-fluorophenyl)methanamine

생성물 1

HCID 668103533-Cyano-1-(4-fluoro-benzyl)-6-hydroxy-7-oxo-1,7-dihydro-pyrazolo[1,5-a]pyrimidine-5-carboxylic acid 4-fluoro-benzylamide수율 37.5%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

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온도
90 °C

실험 절차

Sodium hydride (11.0 mg, 0.367 mmol) was added in one portion to a stirred suspension of 3-Cyano-6-hydroxy-7-oxo-1,7-dihydro-pyrazolo[1,5-a]pyrimidine-5-carboxylic acid 4-fluoro-benzylamide compound with 4-fluorobenzylamine (Example 3.1) (100 mg, 0.306 mmol) in DMF (2 mL) under nitrogen at room temperature. The mixture was stirred for 30 min before p-fluorobenzyl chloride (40 μL, 0.366 mmol) was added and the mixture heated at 90° C. for 2 days. After this time, the reaction was cooled to room temperature and partitioned between ethyl acetate (10 mL) and aqueous hydrochloric acid (1M, 10 mL). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (3×10 mL). The combined organics were washed with water (3×10 mL), brine (10 mL) and then concentrated. The residue was purified by column chromatography (95:5:1 dichloromethane:methanol: aqueous ammonia) to afford the desired product (50 mg, 36%).

후처리

  1. additionwas added
  2. temperatureAfter this time, the reaction was cooled to room temperature
  3. custompartitioned between ethyl acetate (10 mL) and aqueous hydrochloric acid (1M, 10 mL)
  4. customThe organic layer was separated
  5. extractionthe aqueous layer was extracted with ethyl acetate (3×10 mL)
  6. washThe combined organics were washed with water (3×10 mL), brine (10 mL)
  7. concentrationconcentrated
  8. customThe residue was purified by column chromatography (95:5:1 dichloromethane:methanol: aqueous ammonia)

출처 및 근거

ORD 기록
ord-3003eca09637431080807f027926dd36
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08859563B2

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