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Water → 2-chloro-4-{[(3S)-1-ethyl-5-oxo-3-pyrrolidinyl]amino}benzonitrile

HRID 1160410
ノート
印刷プレビュー

反応式

HRID 1160410 の反応式
Cl.[Cl:2][C:3]1[CH:4]=[C:5]([NH:11][C@H:12]([CH2:18][NH:19][CH2:20][CH3:21])[CH2:13][C:14](OC)=[O:15])[CH:6]=[CH:7][C:8]=1[C:9]#[N:10].O.C(=O)(O)[O-].[Na+]>C(OCC)(=O)C>[Cl:2][C:3]1[CH:4]=[C:5]([NH:11][C@H:12]2[CH2:13][C:14](=[O:15])[N:19]([CH2:20][CH3:21])[CH2:18]2)[CH:6]=[CH:7][C:8]=1[C:9]#[N:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 516892Sodium BicarbonateHCID 131728380Methyl (3S)-3-[(3-chloro-4-cyanophenyl)amino]-4-(ethylamino)butanoate, hydrochloride

生成物 1

HCID 595161932-chloro-4-{[(3S)-1-ethyl-5-oxo-3-pyrrolidinyl]amino}benzonitrile収率 84.3%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

Methyl (3S)-3-[(3-chloro-4-cyanophenyl)amino]-4-(ethylamino)butanoate, hydrochloride (4.0 g., 13.5 mmole) was redissolved in ethyl acetate (50 mL). Water was added (50 mL) and 10% sodium bicarbonate was added with stirring to bring the pH to 8.5. The organic layer was concentrated and redissolved in benzene (120 mL). The solution was heated with stirring at 75° C. for 6 h. The solvent was evaporated. The crude product was triturated with Et2O, chilled and the solid filtered to give the titled compound (3.0 g, 84%). LC-MS (ES) m/e 263 (M+H)+.

後処理

  1. additionwas added
  2. concentrationThe organic layer was concentrated
  3. dissolutionredissolved in benzene (120 mL)
  4. temperatureThe solution was heated
  5. stirringwith stirring at 75° C. for 6 h
  6. customThe solvent was evaporated
  7. customThe crude product was triturated with Et2O
  8. temperaturechilled
  9. filtrationthe solid filtered

出典と根拠

ORDレコード
ord-1256a3ac72324cf88b7fdbf627272a99
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07816395B2

反応ノート

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