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Hydrochloric Acid → HCID 59513721、化合物

HRID 1159890
ノート
印刷プレビュー

反応式

HRID 1159890 の反応式
Cl[C:2]1[N:7]=[C:6]([C:8]2[C:9]([C:17]3[CH:18]=[C:19]([NH:23][C:24](=[O:33])[C:25]4[C:30]([F:31])=[CH:29][CH:28]=[CH:27][C:26]=4[F:32])[CH:20]=[CH:21][CH:22]=3)=[N:10][N:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=23)[CH:5]=[CH:4][N:3]=1.[CH3:34][N:35]([CH:37]=[O:38])C.[NH2:39][C:40]1[CH:41]=C(CC(N)=O)[CH:43]=[CH:44][CH:45]=1.Cl.[CH3:51]CO>>[C:37]([NH:35][C:34]1[CH:41]=[C:40]([NH:39][C:2]2[N:7]=[C:6]([C:8]3[C:9]([C:17]4[CH:18]=[C:19]([NH:23][C:24](=[O:33])[C:25]5[C:30]([F:31])=[CH:29][CH:28]=[CH:27][C:26]=5[F:32])[CH:20]=[CH:21][CH:22]=4)=[N:10][N:11]4[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=34)[CH:5]=[CH:4][N:3]=2)[CH:45]=[CH:44][CH:43]=1)(=[O:38])[CH3:51]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 5

HCID 313Hydrochloric AcidHCID 702EthanolHCID 6228DimethylformamideHCID 1088232-(3-Aminophenyl)acetamideHCID 59513803N-{3-[3-(2-Chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}-2,6-difluorobenzamide

生成物 1

HCID 59513721HCID 59513721、化合物収率 26%

反応条件

温度
70 °C

実験手順

To a slurry of N-{3-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}-2,6-difluorobenzamide (133 mg, 0.288 mmol.) in 1 mL of EtOH/0.25 mL of DMF, N/(3-aminophenyl)acetamide (71 mg, 0.32 mmol.) and 5 uL of conc. HCl, the reaction contents were heated to 70° C. After heating for 18 h, the reaction was cooled to rt, partitioned the reaction with EtOAc and sat. aq. NaHCO3. The layers were separated, extracted the aqueous layer with EtOAc (2×10 mL), the organic layers were pooled, dried over MgSO4, filtered, reduced in vacuo onto silica. Purification via ISCO (hexanes:EtOAc) to afforded a white solid, 43 mg (26% yield). 1H NMR (400 MHz, d6-DMSO): δ 10.92 (s, 1H); 9.81 (s, 1H); 9.52 (s, 1H); 8.81 (d, J=7 Hz, 1H); 8.54 (d, J=9 Hz, 1H); 8.21 (d, J=6, 1H); 7.94 (d, J=16 Hz, 2H); 7.81 (d, J=9 Hz, 1H); 7.58-7.54 (m, 1H); 7.47-7.41 (m, 2H); 7.34 (t, J=10 Hz, 2H); 7.25-7.09 (m, 5H): 6.47 (d, J=5 Hz, 1H); 5.72 (s, 1H); 1.99 (s, 3H). HRMS calculated C32H24F2N7O2 [M+H]+ 576.1960, found 576.1945.

後処理

  1. temperatureAfter heating for 18 h
  2. temperaturethe reaction was cooled to rt
  3. custompartitioned
  4. customthe reaction with EtOAc and sat. aq. NaHCO3
  5. customThe layers were separated
  6. extractionextracted the aqueous layer with EtOAc (2×10 mL)
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. customPurification via ISCO (hexanes:EtOAc)
  10. customto afforded a white solid, 43 mg (26% yield)

出典と根拠

ORDレコード
ord-442bc44dd20146dea53093de89b0cdf3
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07812022B2

反応ノート

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