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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926907Generated: November 1, 2026

Hydrochloric Acid → HCID 58016784, compound

https://huagongshe.com/reaction/1926907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant(2R,3R)-ButanediolHCID 225936—
Reactant4-Chloro-5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidineHCID 58016815—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 58016784HCID 58016784—

Reaction Conditions

Temperature70 °C

Reaction Steps

Add 2.4 ml of a 12.5 N sodium hydroxide solution to a solution of 1.34 g (14.8 mmol) (2R,3R)-butane-2,3-diol in 20 ml toluene, 7 ml 1,2-dimethoxyethane and 7 ml water at 70° C. After adding 101 mg (0.30 mmol) tetra-n-butylammonium hydrogensulphate and 1.00 g (2.97 mmol) 4-chloro-5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidine, stir the reaction mixture for 17 h at 70° C. After cooling to room temperature, adjust to pH 7 with concentrated hydrochloric acid. Extract three times with 50 ml dichloromethane each time. Wash the combined organic extracts with satd. sodium chloride solution, dry over sodium sulphate, filter and concentrate by vacuum evaporation. Mix the raw product with methanol, filter, and purify the filtrate by preparative RP-HPLC (gradient: water/acetonitrile). 0.60 g (50% of theor.) of the desired product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183246B2
Source datasetuspto-grants-2012_05
ORD IDord-1cb1ba5667cb49b49f199a0d2d8b60ad
Source noteuspto-grants-2012_05