HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894690Generated: October 29, 2026
Hydrochloric Acid → HCID 13388342, compound
https://huagongshe.com/reaction/894690
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15665156 | HCID 15665156 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13388342 | HCID 13388342 | 98.3% |
Reaction Steps
To a solution of 2-(N-methyl-N-benzylamino)ethyl 2-methyl-4-(3-nitrophenyl)-5-ethoxycarbonyl-6-formyl-1,4-dihydropyridine-3-carboxylate (1.5 g) in ethanol (15 ml) was added sodium borohydride (112 mg) under stirring and ice-cooling, and this mixture was further stirred for 20 minutes at the same temperature. The reaction mixture was adjusted with 0.1 N hydrochloric acid to pH 6 to 7 under ice-cooling, and concentrated under reduced pressure. To the residue was added ethyl acetate and water, and the aqueous layer was further washed with ethyl acetate twice. The extract obtained above and the washings were put together, washed with water, dried over magnesium sulfate, and concentrated under reduced pressure to give an oil (1.48 g) of 2-(N-methyl-N-benzylamino)ethyl 2-methyl-4-(3-nitrophenyl)-5-ethoxycarbonyl-6-hydroxymethyl-1,4-dihydropyridine-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04284634 |
|---|
| Source dataset | uspto-grants-1981_08 |
|---|
| ORD ID | ord-9a7666457f214505b3318afd6ead5c9c |
|---|
| Source note | uspto-grants-1981_08 |
|---|