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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365772Generated: October 30, 2026

Phosphorus tribromide → 4-(2-(Bromomethyl)-5-chlorothiazolo[4,5-d]pyrimidin-7-yl)morpholine

https://huagongshe.com/reaction/1365772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus tribromideHCID 24614—
Reactant(5-Chloro-7-morpholinothiazolo[4,5-d]pyrimidin-2-yl)methanolHCID 57685397—
SolventBenzeneHCID 241—
Product4-(2-(Bromomethyl)-5-chlorothiazolo[4,5-d]pyrimidin-7-yl)morpholineHCID 57685396—

Reaction Steps

To a solution of (5-chloro-7-morpholinothiazolo[4,5-d]pyrimidin-2-yl)methanol 56 (100 mg, 0.4 mmol) in benzene (3.0 mL) at 0° C. was added PBr3 (30 ΔL, 0.4 mmol). The reaction was heated at reflux for 1 hour. After cooling to room temperature the reaction was quenched by the addition of water. The aqueous layer was extracted with EtOAc. The combined organics were dried over Na2SO4 and concentrated in vacuo. The crude 4-(2-(bromomethyl)-5-chlorothiazolo[4,5-d]pyrimidin-7-yl)morpholine 57 did not require further purification (x mg, x %). MS (Q1)×(M)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893059B2
Source datasetuspto-grants-2011_02
ORD IDord-676b8f41931d46ab8dfe0799b569829e
Source noteuspto-grants-2011_02