HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979372Generated: October 29, 2026
(+)-1-tert-Butylcarbonylmethyl-2-oxo-3-[(2S)-[2-(N-phenylthioureido)-3-phenylpropionyl]amino]-5-phenyl-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine → 1-tert-butylcarbonylmethyl-2-oxo-3-amino-5-phenyl-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine
https://huagongshe.com/reaction/1979372
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (+)-1-tert-Butylcarbonylmethyl-2-oxo-3-[(2S)-[2-(N-phenylthioureido)-3-phenylpropionyl]amino]-5-phenyl-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine | HCID 20657782 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 1-tert-butylcarbonylmethyl-2-oxo-3-amino-5-phenyl-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine | HCID 21201941 | 99.3% |
Reaction Steps
(−)-1-tert-Butylcarbonylmethyl-2-oxo-3-[(2S)-[2-(N-phenylthioureido)-3-phenylpropionyl]amino]-5-phenyl-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (2.50 g) was dissolved in trifluoroacetic acid (30 ml), the solution was stirred at 50° C. for one hour. The reaction mixture was concentrated under reduced pressure, the residue was dissolved in methanol (50 ml), concentrated hydrochloric acid (20 ml) was added, and refluxed for one hour. The resultant mixture was concentrated under reduced pressure, neutralized with saturated aqueous sodium bicarbonate, and extracted with methylene chloride. The organic layer was dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography(chloroform:ethyl acetate=20:1), to thereby obtain 1.40 g of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06239131B1 |
|---|
| Source dataset | uspto-grants-2001_05 |
|---|
| ORD ID | ord-6bbe6154e426459bb8c124895afc2d06 |
|---|
| Source note | uspto-grants-2001_05 |
|---|