Phosphorus sulfide (P2S5) → HCID 20361194, compound

HRID 441370Notes

Reaction equation

HRID 441370 reaction equation
[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

Participants

4

Procedure

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.

Workup

  1. temperaturewarmed, under nitrogen, at 110°-120° C. for 1 hour
  2. temperaturecooled
  3. concentrationconcentrated in vacuo
  4. customResidual pyridine was removed by the successive addition of xylene and toluene to the residue with concentration
  5. additionafter each addition
  6. additionThe resulting residue was mixed with dilute sodium carbonate
  7. extractionextracted with chloroform
  8. extractionThe chloroform extract
  9. washwas washed with brine
  10. dry with materialdried over anhydrous sodium sulfate
  11. concentrationconcentrated
  12. customThe residue was crystallized

Sources & evidence

ORD record
ord-dad3beb6ed154aa98855d442828ed987
Source dataset
uspto-grants-1977_08
Patent number
US04039551

Reaction notes

Loading…