HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl formate → N-[2-(Benzyloxy)-5-(pyridine-2-carbonyl)phenyl]formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | [3-Amino-4-(benzyloxy)phenyl](pyridin-2-yl)methanone | HCID 53880974 | — |
| Product | N-[2-(Benzyloxy)-5-(pyridine-2-carbonyl)phenyl]formamide | HCID 53784995 | — |
Reaction Steps
A mixture of 10.0 g (32.8 mmol) of 3-amino-4-benzyloxyphenyl 2-pyridyl ketone and 200 ml of ethyl formate is refluxed with stirring for 24 hours. The reaction mixture is evaporated and the residue is dissolved in methylene chloride, then is washed with dilute HCl and saturated saline solution. The dried organic phase is evaporated to give 4-benzyloxy-3-formamidophenyl 2-pyridyl ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03985887 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-1f66b970818545b9a5dd8f3b7f9dc50e |
| Source note | uspto-grants-1976_10 |