HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 68970853, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 68968712 | HCID 68968712 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68970853 | HCID 68970853 | 91.4% |
Reaction Steps
To a solution of the above amine (462 mg, 1.02 mmol) in CH2Cl2 (10 mL) were added Et3N (0.45 mL, 3.23 mmol) followed by acetic anhydride (0.20 mL, 2.12 mmol) and the mixture was stirred at room temperature overnight to afford 4-[[4-(acetylamino-methyl)-phenyl]-(3-cyano-benzyl)-amino]-piperidine-1-carboxylic acid benzyl ester as a white solid (463 mg, 91%) following work-up and purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07491735B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-d6e8bc8898164697b1bde0d83699b11a |
| Source note | uspto-grants-2009_02 |