Cesium carbonate → (S)-tert-butyl 3-(2-(7-(2-methoxyethoxy)imidazo[1,2-a]pyridin-3-yl)quinolin-8-ylamino)pyrrolidine-1-carboxylate

HRID 1095670ノート

反応式

HRID 1095670 の反応式
Br[C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([C:12]1[N:16]3[CH:17]=[CH:18][C:19]([O:21][CH2:22][CH2:23][O:24][CH3:25])=[CH:20][C:15]3=[N:14][CH:13]=1)[CH:8]=[CH:7]2.[NH2:26][C@@H:27]1[CH2:31][CH2:30][N:29]([C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33])[CH2:28]1.C([O-])([O-])=O.[Cs+].[Cs+].C1C=CC(P(C2C(C3C(P(C4C=CC=CC=4)C4C=CC=CC=4)=CC=C4C=3C=CC=C4)=C3C(C=CC=C3)=CC=2)C2C=CC=CC=2)=CC=1>C1(C)C=CC=CC=1.CC([O-])=O.CC([O-])=O.[Pd+2].ClCCl>[CH3:25][O:24][CH2:23][CH2:22][O:21][C:19]1[CH:18]=[CH:17][N:16]2[C:12]([C:9]3[CH:8]=[CH:7][C:6]4[C:11](=[C:2]([NH:26][C@H:27]5[CH2:31][CH2:30][N:29]([C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33])[CH2:28]5)[CH:3]=[CH:4][CH:5]=4)[N:10]=3)=[CH:13][N:14]=[C:15]2[CH:20]=1

参加物

8

反応条件

温度
100 °C

実験手順

A stream of argon was passed through a mixture of 8-bromo-2-(7-(2-methoxyethoxy)-imidazo[1,2-a]pyridin-3-yl)quinoline (0.100 g, 0.2511 mmol), (R)-tert-butyl 3-aminopyrrolidine-1-carboxylate (0.05537 ml, 0.3264 mmol), Cs2CO3 (0.1145 g, 0.3515 mmol), Pd(OAc)2 (0.01127 g, 0.05022 mmol) and rac-BINAP (0.01564 g, 0.02511 mmol) in toluene (1 mL) for 15 minutes. The mixture was heated to 100° C. for 18 hours. The mixture was then allowed to cool to ambient temperature and dichloromethane was added. After stirring 30 minutes, the resulting mixture was filtered and the filtrate was concentrated to yield the title compound as an oil. MS APCI (+) m/z 504.1 (M+1) detected.

後処理

  1. temperatureto cool to ambient temperature
  2. filtrationthe resulting mixture was filtered
  3. concentrationthe filtrate was concentrated

出典と根拠

ORDレコード
ord-acfa1ff443ab40f290df50ff6e5d5270
出典データセット
uspto-grants-2012_03
特許番号
US08138181B2

反応ノート

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