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Phosphorus sulfide (P2S5) → HCID 20361194、化合物

HRID 1679577
ノート
印刷プレビュー

反応式

HRID 1679577 の反応式
[CH3:1][S:2][C:3]1[CH:4]=[CH:5][C:6]2[NH:12][C:11](=O)[CH2:10][N:9]=[C:8]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=3)[C:7]=2[CH:20]=1.P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:22]>N1C=CC=CC=1>[CH3:1][S:2][C:3]1[CH:4]=[CH:5][C:6]2[NH:12][C:11](=[S:22])[CH2:10][N:9]=[C:8]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=3)[C:7]=2[CH:20]=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

4

反応物 2

HCID 14817Phosphorus sulfide (P2S5)HCID 203612567-(Methylsulfanyl)-5-(pyridin-2-yl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one

生成物 1

HCID 20361194HCID 20361194、化合物

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

反応条件

温度
115 °C

実験手順

A stirred solution of 7-methylthio-1,3-dihydro-5-(2-pyridyl)-2H-1,4-benzodiazepin-2-one (0.0206 mole) in dry pyridine (400 ml.) was treated with phosphorus pentasulfide (5.05 g.), warmed, under nitrogen, at 110-120° C. for 1 hour, cooled and concentrated in vacuo. Residual pyridine was removed by the successive addition of xylene and toluene to the residue with concentration after each addition. The resulting residue was mixed with dilute sodium carbonate and extracted with chloroform. The chloroform extract was washed with brine, dried over anhydrous sodium sulfate and concentrated. The residue was crystallized to give 7-methylthio-1,3-dihydro-5-(2-pyridyl)-2H-1,4-benzodiazepine-2-thione.

後処理

  1. temperaturecooled
  2. concentrationconcentrated in vacuo
  3. customResidual pyridine was removed by the successive addition of xylene and toluene to the residue with concentration
  4. additionafter each addition
  5. additionThe resulting residue was mixed with dilute sodium carbonate
  6. extractionextracted with chloroform
  7. extractionThe chloroform extract
  8. washwas washed with brine
  9. dry with materialdried over anhydrous sodium sulfate
  10. concentrationconcentrated
  11. customThe residue was crystallized

出典と根拠

ORDレコード
ord-174d39762db24f7cb8b7cbbcebc7a318
出典データセット
uspto-grants-1978_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04081452

反応ノート

読み込み中…

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