Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591596Generated: November 4, 2026

Triethylamine → HCID 60139992, compound

https://huagongshe.com/reaction/1591596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Pyrimidinamine, 6-chloro-5-nitro-HCID 101229—
Reactant(1S,2R,3S,5S)-3-Amino-5-(hydroxymethyl)-1,2-cyclopentanediolHCID 11887845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 60139992HCID 6013999260.3%

Reaction Steps

To a solution of 4-amino-6-chloro-5-nitropyrimidine (320 mg, 1.83 mmol) in N,N-dimethyl formamide (5 mL) and triethylamine (512 μL, 3.67 mmol) was added (1S,2R,3S,5S)-3-Amino-5-hydroxymethyl-cyclopentane-1,2-diol (293 mg, 2.02 mmol). The mixture was stirred at room temperature and monitored by thin layer chromatography until starting material was no longer detected. The reaction mixture was diluted with water (20 mL) and extracted with diethyl ether (2×10 mL). The organic extract was washed with saturated aqueous sodium chloride (20 mL), dried over MgSO4, filtered and concentrated in vacuo to give the crude product. The product was recrystallized from hot methanol/water to give a 315 mg of (1S,2R,3S,5S)-3-(6-amino-5-nitro-pyrimidin-4-ylamino)-5-hydroxymethyl-cyclopentane-1,2-diol as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291603B2
Source datasetuspto-grants-2007_11
ORD IDord-10f58d31eaab462cbe1452ac20da8d24
Source noteuspto-grants-2007_11