HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 118677393, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 118677428 | HCID 118677428 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 118677393 | HCID 118677393 | 197.4% |
Reaction Steps
To tert-butyl N-[(1S)-2-[[(1S)-2-[(2S,4S)-2-(benzylcarbamoyl)-4-[[4-[(3S)-5-[(6-bromo-2-methoxy-1-naphthyl)methyl]-3-[[(2S)-2-[tert-butoxycarbonyl(methyl)amino]propanoyl]amino]-4-oxo-2,3-dihydro-1,5-benzodiazepine-1-carbonyl]benzoyl]amino]pyrrolidin-1-yl]-1-cyclohexyl-2-oxo-ethyl]amino]-1-methyl-2-oxo-ethyl]-N-methyl-carbamate (45 mg, 0.035 mmol) in methanol (2 mL) at room temperature was added acetyl chloride (25 μL, 0.035 mmol) dropwise. The mixture was allowed to stand at room temperature. After 16 h the mixture was concentrated and the residue was triturated with acetonitrile to give the title compound (40 mg, 98%) as a tan solid. MS: m/z 1085 (MH+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409888B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-645d80c8cc554e4c8e86077b9be90127 |
| Source note | uspto-grants-2016_08 |