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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032698Generated: November 1, 2026

Sodium borohydride → HCID 14856037, compound

https://huagongshe.com/reaction/1032698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13784152HCID 13784152—
SolventEthanolHCID 702—
ProductHCID 14856037HCID 1485603730%

Reaction Steps

Sodium borohydride (2.24 g) was added to 8.0 g of 2-(4-benzylpiperazino)-5,6-dihydro-7-methyl-6-oxo-(7H)pyrrolo[2,3-d]pyrimidine (produced in accordance with Referential Example 54 of Japanese Laid-Open Patent Publication No. 140568/1986) and 400 ml of ethanol, and the mixture was heated under reflux for 1.5 hours. The reaction mixture was concentrated. The residue was mixed with water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography (methanol:chloroform=1:10), and recrystallized from toluene to give 2.4 g (yield 30%) of 2-(4-benzylpiperazino)-5-(2-hydroxyethyl)-4-methylaminopyrimidine as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04959368
Source datasetuspto-grants-1990_09
ORD IDord-f0ba549067474c01bad91cb60cf20712
Source noteuspto-grants-1990_09