HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258107Generated: October 29, 2026
Phenyl Isothiocyanate → HCID 178516744, compound
https://huagongshe.com/reaction/258107
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenyl Isothiocyanate | HCID 7673 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178511769 | HCID 178511769 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178516744 | HCID 178516744 | 179.4% |
Reaction Steps
To a mixture of (3S)-3-[((2S)-2-amino-3phenylpropanoyl)amino]-1,3-dihydro-5-phenyl-1 -[(1H-tetrazol-5-yl)methyl]-2H-1,4-benzodiazepin-2-one (12 g) and triethylamine (3.83 ml) in tetrahydrofuran (240 ml) was added phenyl isothiocyanate (2.99 ml) at room temperature. After stirring for 4 hours at room temperature, the solvent of the reaction mixture was evaporated under reduced pressure. Hydrochloric acid was added to the residue, and then the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was crystallized from ether to give (3S)-3-[[(2S)-2-[N'-phenyl)thioureido]-3-phenylpropanoyl]amino ]1,3-dihydro-5-phenyl-1-[(1H-tetrazol-5-yl)methyl]-2H-1,4-benzodiazepin-2-one (14.26 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05264433 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-684449740e23412c9b5cc4a2e4478e44 |
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| Source note | uspto-grants-1993_11 |
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