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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032221Generated: October 25, 2026

Sodium borohydride → HCID 178519774, compound

https://huagongshe.com/reaction/1032221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178498586HCID 178498586—
SolventEthanolHCID 702—
ProductHCID 178519774HCID 17851977491.9%

Reaction Steps

In 4 liters of ethanol was suspended 48.94 g of 7-hydroxy-2-hydroxymethyl-5-methoxycarbonyl-s-triazolo[1,5-a]pyrimidine, and 33 g of sodium borohydride was added little by little thereto and then the mixture was stirred at room temperature for 3 hours and then refluxed for 4 hours. A residue obtained by removing ethanol was dissolved in 2 liters of water, and 500 ml of Amberlite IRC-50 (H+) (trade name) was added thereto and stirred. Subsequently, the mixture was filtered and after removing water from the filtrate, 500 ml of methanol was added to the filtrate and the mixture was stirred. Then, methanol was removed from the mixture to obtain a residue. These procedures were repeated three times. Then, 500 ml of ethanol was added to the residue and the mixture was condensed. Precipitated crystal was collected by filtration, washed with ethanol and dried to obtain 39.35 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04956462
Source datasetuspto-grants-1990_09
ORD IDord-864400f22b1e4ec38dd6b3b691150c12
Source noteuspto-grants-1990_09