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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366320Generated: November 3, 2026

Cesium carbonate → {3,5-Dichloro-4-[7-fluoro-4-(6-hydroxymethylpyrimidin-4-ylamino)-thiazolo[5,4-c]pyridin-2-yl]phenyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2366320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant(6-Aminopyrimidin-4-yl)methanolHCID 21934615—
Reactant[3,5-Dichloro-4-(4-chloro-7-fluorothiazolo[5,4-c]pyridin-2-yl)phenyl]-carbamic acid tert-butyl esterHCID 86669030—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Product{3,5-Dichloro-4-[7-fluoro-4-(6-hydroxymethylpyrimidin-4-ylamino)-thiazolo[5,4-c]pyridin-2-yl]phenyl}-carbamic acid tert-butyl esterHCID 6680163358%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of [3,5-dichloro-4-(4-chloro-7-fluorothiazolo[5,4-c]pyridin-2-yl)phenyl]-carbamic acid tert-butyl ester (150 mg, 0.33 mmol) in dioxane (5 mL), was added (6-aminopyrimidin-4-yl)methanol (45 mg, 0.36 mmol), XantPhos (19.4 mg, 0.033 mmol) and Cs2CO3 (218.3 mg, 0.67 mmol). The resultant mixture was degassed with argon for 10 minutes before Pd2(dba)3 (57.7 mg, 0.063 mmol) was added and the reaction mixture was heated at 100° C. for 18 hours in a sealed vial. After cooling to room temperature, the reaction mixture was filtered through Celite® washing with EtOAc (5 mL). The resultant residue was purified by column chromatography on silica gel eluting with 0-80% EtOAc in cyclohexane to afford the title compound as a white foam (102 mg, 58%). LCMS (Method D): RT=3.35 min, m/z: 538 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697708B2
Source datasetuspto-grants-2014_04
ORD IDord-cf8eb076ab1c43d08bdc442bda6afb3e
Source noteuspto-grants-2014_04