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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406331Generated: October 28, 2026

Triethylamine → Pyrimidine-5-carboxylic acid-{1-[4-(4-chloro-2-fluoro-phenoxy)-3-fluoro-benzylcarbamoyl]-cyclopropyl}-amide hydrochloride

https://huagongshe.com/reaction/1406331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant4-(4-Chloro-2-fluoro-phenoxy)-3-fluoro-benzylamineHCID 58487907—
Reactant1-[(Pyrimidine-5-carbonyl)-amino]cyclopropanecarboxylic acidHCID 59496291—
SolventTetrahydrofuranHCID 8028—
ProductPyrimidine-5-carboxylic acid-{1-[4-(4-chloro-2-fluoro-phenoxy)-3-fluoro-benzylcarbamoyl]-cyclopropyl}-amide hydrochlorideHCID 6744738656%

Reaction Steps

0.5 mL (3.6 mmol) of triethylamine, 0.433 g (1.35 mmol) of TBTU and 325.5 mg (1.2 mmol) of 4-(4-chloro-2-fluoro-phenoxy)-3-fluoro-benzylamine were added to a solution of 250 mg (1.2 mmol) of 1-[(pyrimidine-5-carbonyl)-amino]-cyclopropanecarboxylic acid (from 1b) in 15 mL tetrahydrofuran and the mixture was stirred overnight at ambient temperature. Then the mixture was evaporated to dryness and the crude product thus obtained was purified by chromatography. The purified product was dissolved in approx. 4 mL ethyl acetate and the dropwise addition of ethereal hydrochloric acid solution caused the hydrochloride to precipitate out, which was then filtered off and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916589B2
Source datasetuspto-grants-2014_12
ORD IDord-dc8f9206c31b4873a9152464f0952e6f
Source noteuspto-grants-2014_12