HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 22716657, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22716682 | HCID 22716682 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22716657 | HCID 22716657 | — |
Reaction Steps
To an ethanol solution of ethyl 1-[4-(3-chlorophenyl)-1-ethyl-7-formyl-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]piperidine-4-carboxylate was added sodium borohydride under ice cooling, followed by stirring for 15 minutes. Thereafter, the reaction mixture was worked up and purified in a usual manner to obtain ethyl 1-[4-(3-chlorophenyl)-1-ethyl-7-hydroxymethyl-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]piperidine-4-carboxylate as a yellow oily substance. MS: 470.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06740662B1 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-8ece45f3e3f0413f9c83cb674617da0e |
| Source note | uspto-grants-2004_05 |