HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283406Generated: October 31, 2026
Chloroacetyl chloride → HCID 89545092, compound
https://huagongshe.com/reaction/2283406
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 117874973 | HCID 117874973 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89545092 | HCID 89545092 | 95.4% |
Reaction Steps
Step 4 Chloroacetyl chloride (0.323 ml, 4.05 mmol) was added to a mixture of tert-butyl N-[(1R)-1-(3-{[4-amino-3-(benzyloxy)phenyl]carbonyl}-4-chloro-2-fluorophenyl)propyl]carbamate (1.6 g, 3.12 mmol), triethylamine (0.651 ml, 4.68 mmol) and dichloromethane (30 ml) at room temperature. After 30 minutes a small additional portion of chloroacetyl chloride was added and in 60 minutes the reaction was complete. The reaction mixture was washed with dilute citric acid solution and dilute sodium bicarbonate and then concentrated. The residue was purified on silica eluting with 30-70% ethyl acetate/petrol to furnish tert-butyl N-[(1R)-1-(3-{[3-(benzyloxy)-4-(2-chloroacetamido)-phenyl]-carbonyl}-4-chloro-2-fluorophenyl)propyl]carbamate as a yellow oil (1.754 g). [M−H]−=587
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145354B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-ab3c982c0fa94df3b13ba445c702f6a9 |
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| Source note | uspto-grants-2015_09 |
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