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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252260Generated: November 3, 2026

Sodium borohydride → HCID 70416706, compound

https://huagongshe.com/reaction/1252260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantDichloromethane ethylacetateHCID 21226138—
ReactantHCID 70416973HCID 70416973—
SolventIsopropanolHCID 3776—
ProductHCID 70416706HCID 7041670682.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742069
Source datasetuspto-grants-1988_05
ORD IDord-ea6416f1defd4c32b3c5d38916e1259c
Source noteuspto-grants-1988_05