Triethylamine → (2R,4R)-2-[2-Fluoro-4-(3-methyl-pyrazol-1-yl)-phenylcarbamoyl]-4-methoxy-pyrrolidine-1-carboxylic acid tert-butyl ester

HRID 1796291ノート

反応式

HRID 1796291 の反応式
[C:1]([O:5][C:6]([N:8]1[CH2:12][C@H:11]([O:13][CH3:14])[CH2:10][C@@H:9]1[C:15]([OH:17])=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].[F:18][C:19]1[CH:24]=[C:23]([N:25]2[CH:29]=[CH:28][C:27]([CH3:30])=[N:26]2)[CH:22]=[CH:21][C:20]=1[NH2:31].CCOC1N(C(OCC)=O)C2C(=CC=CC=2)C=C1.CCN(CC)CC>C(Cl)(Cl)Cl>[C:1]([O:5][C:6]([N:8]1[CH2:12][C@H:11]([O:13][CH3:14])[CH2:10][C@@H:9]1[C:15](=[O:17])[NH:31][C:20]1[CH:21]=[CH:22][C:23]([N:25]2[CH:29]=[CH:28][C:27]([CH3:30])=[N:26]2)=[CH:24][C:19]=1[F:18])=[O:7])([CH3:2])([CH3:3])[CH3:4]

参加物

6

実験手順

(2R,4R)-4-methoxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (0.350 g, 1.427 mmol), aniline 1 (0.273 g, 1.427 mmol) and EEDQ (0.529 g, 2.140 mmol) were dissolved in CHCl3 (30 mL). Et3N (0.6 mL, 4.281 mmol) was added and the reaction mixture was heated at reflux for 18 h. The mixture was allowed to cool and diluted with CHCl3 (100 mL) and washed with 5% HCl, 0.5 N NaOH, water and brine (40 mL each), the organic extract was dried over MgSO4, filtered and the solvent removed to give a pale tan foam. The crude product was used for the next step without purification. MS: APCI (AP+): 419.2 (M)+, (AP−): 417.2 (M)−.

後処理

  1. temperaturethe reaction mixture was heated
  2. temperatureat reflux for 18 h
  3. temperatureto cool
  4. washwashed with 5% HCl, 0.5 N NaOH, water and brine (40 mL each)
  5. extractionthe organic extract
  6. dry with materialwas dried over MgSO4
  7. filtrationfiltered
  8. customthe solvent removed
  9. customto give a pale tan foam
  10. customThe crude product was used for the next step without purification

出典と根拠

ORDレコード
ord-bd86491f7bb44356aaf45e5a884e307e
出典データセット
uspto-grants-2006_04
特許番号
US07030141B2

反応ノート

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