HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 70416706, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Dichloromethane ethylacetate | HCID 21226138 | — |
| Reactant | HCID 70416973 | HCID 70416973 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 70416706 | HCID 70416706 | 82.7% |
Reaction Steps
Analogously to Example 18, a solution of 1.56 g of 1,4-dihydro-5-[(isopropylsulfamoyl)acetyl]-2,6-dimethyl-4-(3-nitrophenyl)nicotinic acid 2,2,2-trifluoroethyl ester in 15 ml of isopropanol was treated with 0.12 g (3 mmol) of sodium borohydride. After chromatography with methylene chloride/ethyl acetate (4:1) as the elution agent there were obtained 1.25 g of 1,4-dihydro-5-[(E)-2-(isopropylsulfamoyl)vinyl]-2,6-dimethyl-4-(3-nitrophenyl)nicotinic acid 2,2,2-trifluoroethyl ester in the form of yellow crystals, m.p. 180°-182°. Recrystallization from isopropanol did not increase the melting point.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04742069 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-ea6416f1defd4c32b3c5d38916e1259c |
| Source note | uspto-grants-1988_05 |