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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256775Generated: October 26, 2026

Methanol → HCID 19785542, compound

https://huagongshe.com/reaction/256775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDiethyl EtherHCID 3283—
ReactantBromineHCID 24408—
ReactantMethylthioureaHCID 2723704—
Reactant5-(2-Fluoro-4-biphenylyl)-4-oxohexanoic acidHCID 19785566—
ProductHCID 19785542HCID 1978554235%

Reaction Steps

To an ice-cooled solution of 5-(2-fluoro-4-biphenylyl)-4-oxohexanoic acid (500 mg, 1.52 mmoles) in diethyl ether (10 ml) was added dropwise bromine (243 mg, 1.52 mmoles) and the resulting mixture was stirred at room temperature for 3.5 hours. The reaction mixture was concentrated under reduced pressure. A mixture of the afforded residue, N-methylthiourea (164 mg, 1.82 mmoles) and methanol was stirred at 50° C. for 2 hours and concentrated under reduced pressure. The residue was partitioned between ethyl acetate and aqueous sodium bicarbonate. The organic layer was washed with water, dried over sodium sulfate and concentrated under reduce pressure. Purification of the residue by medium pressure silica gel column chromatography gave the desired ethyl 2-(4-(1-(2-fluoro-4-biphenylyl)ethyl)-2-methylamino-5-thiazolyl)acetate (209 mg, 0.524 mmole, yield 35%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258396
Source datasetuspto-grants-1993_11
ORD IDord-4d4587232178424baa5731f6b33f3622
Source noteuspto-grants-1993_11