HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073720Generated: November 3, 2026
Trifluoroacetic acid → HCID 57293116, compound
https://huagongshe.com/reaction/1073720
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | HCID 54503167 | HCID 54503167 | — |
| Reactant | HCID 56985990 | HCID 56985990 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57293116 | HCID 57293116 | — |
Reaction Steps
A mixture of a mixture (0.66 g) of (3R)-1-[2-((2R)-2-tert-butoxycarbonylamino-2-benzhydryloxycarbonylethylthio)ethyl]-1,3-dihydro-3-(2-indolylcarbonylamino) -5-phenyl-2H-1,4-benzodiazepine-2-one and (3S)-1-[2-((2R)-2-tert-butoxycarbonylamino-2benzhydryloxycarbonylethylthio)ethyl]-1,3-dihydro-3-(2-indolylcarbonylamino) -5-phenyl-2H-1,4-benzodiazepine-2-one, anisole (0.6 ml), trifluoroacetic acid (1.5 ml) and dichloromethane (15 ml) was stirred for 3.0 hours at room temperature. After removal of the solvent, the residue was mixed with ethyl acetate (50 ml) and water (50 ml). The mixture was adjusted to pH 6-7 with 5% aqueous solution of sodium bicarbonate under stirring. The organic layer was separated and concentrated. The resultant precipitate was collected by filtration, washed with water and dried to give a mixture (0.20 g) of (3R)-1-[2-((2R)-2-amino-2-carboxyethylthio)ethyl]-1,3-dihydro -3-(2-indolylcarbonylamino -5-phenyl-2H-1,4-benzodiazepine- 2-one and (3S)-1-[2-((2R)-2-amino-2-carboxyethylthio) ethyl]-1,3-dihydro-3-(2-indolylcarbonylamino) -5-phenyl-2H-1,4-benzodiazepine-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04970207 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-3aa78ba134f1440985d1bcd6f7437a28 |
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| Source note | uspto-grants-1990_11 |
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