HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629758Generated: October 30, 2026
Methyl chloroformate → HCID 86726362, compound
https://huagongshe.com/reaction/629758
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86726360 | HCID 86726360 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86726362 | HCID 86726362 | — |
Reaction Steps
To a stirred solution of (2S,3S)-2-amino-3-(4-fluorophenyl)-3-(3,5-difluorophenyl)-N-(5-fluoro-4-(2-((2R,5R)-4-(tert-butyloxycarbonyl)-5-(2,2,2-trifluoroethylaminocarbonyloxymethyl)morpholine-2-yl)ethyl)pyridin-3-yl)propanamide (Example 90, step 5) (64 mg, 0.084 mmol) in 1 mL of CH2Cl2 was added triethylamine (0.047 mL, 0.34 mmol) and methyl chloroformate (0.013 mL, 0.17 mmol). The mixture was stirred at ambient temperature for 1 h, then diluted with CH2Cl2 and washed with aqueous NaHCO3 and brine. The organic phase was dried (MgSO4), filtered, and the solvents were removed in vacuo. The residue was chromatographed on a 12 g SiO2 column using a gradient elution of 0-100% EtOc in hexanes. Fractions containing product were combined and the solvents were removed in vacuo to give a gum. LC MS: RT=1.38 min, M+H=816 (2 min gradient)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09315475B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-66a34173e4f34672a59c8af2511da6fc |
|---|
| Source note | uspto-grants-2016_04 |
|---|