HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 70416825, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Dichloromethane ethylacetate | HCID 21226138 | — |
| Reactant | HCID 70415797 | HCID 70415797 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70416825 | HCID 70416825 | 83.5% |
Reaction Steps
Analogously to Example 18, 1.86 g of 5-[(ethylsulfamoyl)acetyl]-1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)nicotinic acid isopropyl ester were treated with 0.16 g of sodium borohydride in a mixture of 20 ml of isopropanol and 4 ml of dimethylformamide. After chromatography with methylene chloride/ethyl acetate (4:1) as the elution agent there were obtained 1.5 g of 5-[(E)-2-(ethylsulfamoyl)vinyl]-1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)nicotinic acid isopropyl ester in the form of yellow crystals, m.p. 187°-189°. Recrystallization from methylene chloride/ether 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-65e45af608cf4406bdeb4f6f1c0d0e2a |
| Source note | uspto-grants-1988_05 |