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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926975Generated: November 2, 2026

4-{[(2S)-2-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}propyl]-(methyl)amino}butyric acid tert.-butyl ester → (+)-4-{[(2S)-2-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}propyl]-(methyl)amino}butyric acid

https://huagongshe.com/reaction/1926975

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-{[(2S)-2-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}propyl]-(methyl)amino}butyric acid tert.-butyl esterHCID 58016818—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
Product(+)-4-{[(2S)-2-{[6-(2-Fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}propyl]-(methyl)amino}butyric acidHCID 58016840—

Reaction Steps

Dissolve 102 mg (93% purity, 0.19 mmol) 4-{[(2S)-2-{[6-(2-fluorophenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]oxy}propyl](methyl)amino}butyric acid tert.-butyl ester in 2 ml 4 N hydrogen chloride in dioxan and stir for 16 h at RT. After concentrating the reaction solution by evaporation under vacuum, purify the residue by preparative RP-HPLC (gradient: water/acetonitrile). 48 mg (52% 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-8021c50ff605496da3d98a5c09492a1c
Source noteuspto-grants-2012_05