Benzyl Bromide → 2-Phenylmethyl-4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide

HRID 743437ノート

反応式

HRID 743437 の反応式
[CH:1]([CH:4]1[NH:8][S:7](=[O:10])(=[O:9])[NH:6][C:5]1=[O:11])(C)[CH3:2].[C:12]1([CH2:18]Br)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[C:20]1(C)C=CC=CC=1.CN(C=O)C>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC>[C:12]1([CH2:18][N:6]2[C:5](=[O:11])[CH:4]([CH2:1][CH2:2][CH3:20])[NH:8][S:7]2(=[O:10])=[O:9])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

参加物

5

実験手順

Eight grams (44.94 mmol) of 4-isopropyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide, phenylmethyl bromide (8.09 g, 47.2 mmol), and tetrabutylammonium bromide (1.5 g, 4.66 mmol) suspended in toluene/DMF (200 ml/50 ml) was allowed to react at 130° C. for 30 hours. The resulting mixture was cooled, the excess toluene was concentrated in vacuo, and the residue was diluted with 200 ml of water and extracted with ether/ethyl acetate (4:1, 700 ml). The organic layer was washed with water and brine, dried and concentrated in vacuo to yield a residue which was purified by flash chromatography to afford 8.6 g (72%) of 2-phenylmethyl-4-isopropyl-1,2,5-thiadiazol-idin-3-one 1,1-dioxide (Formula IX: R1 =H; R2 =isopropyl) as a solid.

後処理

  1. customto react at 130° C. for 30 hours
  2. temperatureThe resulting mixture was cooled
  3. concentrationthe excess toluene was concentrated in vacuo
  4. additionthe residue was diluted with 200 ml of water
  5. extractionextracted with ether/ethyl acetate (4:1, 700 ml)
  6. washThe organic layer was washed with water and brine
  7. customdried
  8. concentrationconcentrated in vacuo
  9. customto yield a residue which
  10. customwas purified by flash chromatography

出典と根拠

ORDレコード
ord-8f905c599f9e42a5ae93696785f40892
出典データセット
uspto-grants-1996_09
特許番号
US05556909

反応ノート

読み込み中…