HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 118677384, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 118677396 | HCID 118677396 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 118677384 | HCID 118677384 | 84% |
Reaction Steps
tert-Butyl N-[(1S)-2-[[(3S)-5-[(6-bromo-2-methoxy-1-naphthyl)methyl]-1-[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]-4-oxo-2,3-dihydro-1,5-benzodiazepin-3-yl]amino]-1-methyl-2-oxo-ethyl]-N-methyl-carbamate (24 mg, 0.018 mmol) and acetyl chloride (6.3 μL, 0.089 mmol) were combined in MeOH (2 mL) and stirred at room temperature overnight. The mixture was concentrated and the residue triturated with acetonitrile to give the title compound (18.3 mg, 84%) as a solid. LC-MS: 1149 [M−H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409888B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-edf88cbcebe0407882a9e868e0ab969e |
| Source note | uspto-grants-2016_08 |