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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633164Generated: October 31, 2026

Sodium borohydride → HCID 58614630, compound

https://huagongshe.com/reaction/633164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58614857HCID 58614857—
SolventEthanolHCID 702—
ProductHCID 58614630HCID 58614630—

Reaction Steps

To 110 mg of methyl 6-(2-chloro-5-(2-methyl-6-(trifluoromethyl)nicotinamido)phenyl)nicotinate at 0° C. in 5 mL of EtOH was slowly added 148 mg of Sodium Borohydride. The reaction was subsequently refluxed for 1 hour until complete, quenched with water and extracted with Ethyl Acetate. The organic layer was dried over Magnesium Sulfate, filtered, concentrated and purified by reverse phase HPLC to give pure N-(4-chloro-3-(5-(hydroxymethyl)pyridin-2-yl)phenyl)-2-methyl-6-(trifluoromethyl)nicotinamide. MS (Q1) 422.1 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321761B2
Source datasetuspto-grants-2016_04
ORD IDord-8b12e68a290148eb806a36bc4a8be160
Source noteuspto-grants-2016_04