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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330801Generated: October 29, 2026

Triphenylphosphine → 3-{3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]benzyl}-5-trifluoromethyl-3H-benzothiazol-2-one

https://huagongshe.com/reaction/330801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant5-(Trifluoromethyl)benzo[d]thiazol-2(3H)-oneHCID 13227340—
Reactant{3-[5-(3-Dimethylaminopropoxy)pyrimidin-2-yl]phenyl}methanolHCID 59484942—
Product3-{3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]benzyl}-5-trifluoromethyl-3H-benzothiazol-2-oneHCID 46846628—

Reaction Steps

A suspension of 114 mg (0.52 mmol) of 5-trifluoromethyl-3H-benzothiazol-2-one, 150 mg (0.52 mmol) of {3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]phenyl}methanol and 261 mg (0.78 mmol) of polymer-bound triphenylphosphine (3mmol/g) is shaken at room temperature for 30 min. 178 mg (0.78 mmol) of di-tert-butyl azodicarboxylate are added to the suspension, and, after the mixture has been stirred at room temperature for 24 h, 50 mg (0.15 mmol) of polymer-bound triphenylphosphine (3 mmol/g) and 35 mg (0.15 mmol) of di-tert-butyl azodicarboxylate are again present and shaken at room temperature for 2 h. The reaction mixture is filtered, the filtrate is evaporated to dryness, and the residue is purified by means of preparative HPLC. The product is in the form of the trifluoroacetate; ESI: 489 (M+H); Rt.=2.81 min (method A);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877751B2
Source datasetuspto-grants-2014_11
ORD IDord-f937e100eef7407481c2c51dceb0527a
Source noteuspto-grants-2014_11