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Sodium hydride → 1-(3-Chloro-4-cyano-2-methylbenzyl)-2-oxo-octahydrocyclopenta[b]-pyrrol-4-yl benzoate

HRID 642750
ノート
印刷プレビュー

反応式

HRID 642750 の反応式
[C:1]([O:9][CH:10]1[CH:17]2[CH:13]([C:14](=[O:18])[NH:15][CH2:16]2)[CH2:12][CH2:11]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OC1C2C(NC(=O)C2)CC1)(=O)C1C=CC=CC=1.[H-].[Na+].Br[CH2:40][C:41]1[CH:48]=[CH:47][C:44]([C:45]#[N:46])=[C:43]([Cl:49])[C:42]=1[CH3:50]>C1COCC1.CN(C=O)C>[C:1]([O:9][CH:10]1[CH:17]2[CH:16]([N:15]([CH2:40][C:41]3[CH:48]=[CH:47][C:44]([C:45]#[N:46])=[C:43]([Cl:49])[C:42]=3[CH3:50])[C:14](=[O:18])[CH2:13]2)[CH2:12][CH2:11]1)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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

7

反応物 4

HCID 24758Sodium hydrideHCID 592595601-Oxo-octahydrocyclopenta[c]pyrrol-4-yl benzoateHCID 592595712-Oxo-octahydrocyclopenta[b]pyrrol-4-yl benzoateHCID 685774134-(Bromomethyl)-2-chloro-3-methylbenzonitrile

生成物 1

HCID 592595681-(3-Chloro-4-cyano-2-methylbenzyl)-2-oxo-octahydrocyclopenta[b]-pyrrol-4-yl benzoate

試薬・触媒・溶媒 2

HCID 6228
Dimethylformamide
溶媒
HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

To a solution containing mixtures of compound 1I and 1J (170 mg, 0.69 mmol, different batch than previous lot in example 1) in anhydrous THF (4 mL) and anhydrous DMF (4 mL) was added sodium hydride (27.7 mg, 0.69 mmol) at 0° C., and stirred at 0° C. for 45 min. Compound 7C (169 mg, 0.69 mmol) was added at 0° C., the ice-water bath was removed, and the stirring was continued between 0° C. to RT for 2 hr before it was quenched with saturated NH4Cl solution. The mixture was diluted with EtOAc, organic layer was separated, washed with water, dried over MgSO4, and concentrated. Purification by silica gel chromatography (30-100% EtOAc in hexanes) provide the title compound 7D (90 mg) and 7E (151 mg). Compound 7D: (ES) m/z 409 [M+H]+. Compound 7E: (ES) m/z 409 [M+H]+.

後処理

  1. customthe ice-water bath was removed
  2. waitthe stirring was continued between 0° C. to RT for 2 hr before it
  3. customwas quenched with saturated NH4Cl solution
  4. additionThe mixture was diluted with EtOAc, organic layer
  5. customwas separated
  6. washwashed with water
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated
  9. customPurification by silica gel chromatography (30-100% EtOAc in hexanes)

出典と根拠

ORDレコード
ord-b5af524b9b9e4377bc526f9bbd2dd217
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07696241B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート