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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441659Generated: November 1, 2026

Triethylamine → HCID 58878496, compound

https://huagongshe.com/reaction/1441659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
Reactant5-(Benzyloxy)-2-bromoanilineHCID 11000366—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 58878496HCID 58878496—

Reaction Steps

Piperidine-1,4-dicarboxylic acid mono-tert-butyl ester (2.25 g, 9.80 mmol) was dissolved in dry methylene chloride (18 mL) and dry pyridine (2.02 mL). To the reaction mixture was then added thionyl chloride (1.40 g, 11.76 mmol) under nitrogen atmosphere and the reaction mixture was stirred at room temperature for 30 minutes. To the reaction mixture was then added successively, under nitrogen atmosphere, 5-benzyloxy-2-bromo-phenylamine (3.0 g, 10.78 mmol), dry triethylamine (3.50 g, 34.32 mmol), dry methylene chloride (20 mL), 4-(dimethylamino)pyridine (0.12 g, 0.98 mmol) and the reaction mixture was stirred at room temperature for 24 hours. The reaction mixture was then partitioned with aqueous 2N HCl and tert-butyl methyl ether. The organic layer was washed with aqueous 2N HCl, aqueous NaHCO3, brine, dried with Na2SO4, filtered and the solvent evaporated in vacuo to yield a crude oil. The crude oil was recrystallized from ethyl acetate/hexanes to yield the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655670B2
Source datasetuspto-grants-2010_02
ORD IDord-6f97e56dd73f4b2a80d4027365b58b15
Source noteuspto-grants-2010_02