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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429790Generated: November 1, 2026

Ethyl Acetate → 7-(1-aminoethyl)-6-(3,5-difluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one

https://huagongshe.com/reaction/1429790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylphosphineHCID 68983—
Reactant7-(1-azidoethyl)-6-(3,5-difluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-oneHCID 86650065—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product7-(1-aminoethyl)-6-(3,5-difluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-oneHCID 58111409—

Reaction Steps

To a stirred solution of 7-(1-azidoethyl)-6-(3,5-difluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one (0.042 g, 0.12 mmol) in tetrahydrofuran (0.3 mL) and water (0.0873 mL) was added 1.0 M of trimethylphosphine in tetrahydrofuran (0.14 mmol) at room temperature and stirred for 1 hour. To the mixture was added EtOAc and the mixture was extracted twice with 1N HCl. The combined extracts were neutralized with solid sodium bicarbonate, and extracted with methylene chloride. The combined organic layers were washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was used directly in next step (36 mg, 92.7%). LCMS calculated for C15H14F2N3OS (M+H)+: m/z=322.1. Found: 322.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940752B2
Source datasetuspto-grants-2015_01
ORD IDord-d70fb15e04e24423a87b4fcf20bc485b
Source noteuspto-grants-2015_01