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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507775Generated: October 31, 2026

Methyl iodide → HCID 50941769, compound

https://huagongshe.com/reaction/1507775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTriethylamineHCID 8471—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantHCID 178508994HCID 178508994—
ReactantHCID 178509030HCID 178509030—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 50941769HCID 5094176921.6%

Reaction Steps

A solution of N-(2-amino-4,6-dihydroxypyrimidin-5-yl)-3-(4-fluorophenoxy)propanamide (2.5 g, 8.11 mmol) and phosphorus pentasulfide (3.60 g, 16.2 mmol) in dry pyridine (40 ml) was refluxed for 6 hours. After cooling down to room temperature, the precipitate was filtered off, washed with ethylacetate and dried. The crude 5-amino-2-(2-(4-fluorophenoxy)ethyl)-thiazolo[5,4-d]pyrimidine-7-thiol (2.0 g, 6.20 mmol) was redissolved in DMSO (30 ml). Triethylamine (0.85 ml, 6.12 mmol) and iodomethane (0.31 ml, 4.90 mmol) were added. The reaction mixture was stirred for 12 hours at room temperature under a nitrogen atmosphere. The mixture was poured into water and extracted with EtOAc. The combined organic layers were dried over Na2SO4 and the solvents were removed under reduced pressure. The crude residue was purified by chromatography on silica gel (CH2Cl2/MeOH 100:1), yielding the title compound as a light yellow solid (0.45 g, 15% over 2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221822B2
Source datasetuspto-grants-2015_12
ORD IDord-536969c30c9244989263c58add997c8e
Source noteuspto-grants-2015_12