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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054859Generated: October 30, 2026

Triethylamine → HCID 16105789, compound

https://huagongshe.com/reaction/2054859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant4-fluoronaphthalene-1-sulfonyl ChlorideHCID 2774647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 16105789HCID 16105789—

Reaction Steps

4-Fluoro-naphthalene-1-sulfonyl chloride 27 (10.0 g, 40.9 mmol) was dissolved in THF (100 mL) and stirred at room temperature. 4-Amino-piperidine-1-carboxylic acid tert-butyl ester (8.19 g, 40.9 mmol) and triethylamine (4.14 g, 5.75 mL, 40.9 mmol) were added and the reaction was stirred overnight at room temperature. The solvent was removed in vacuo. Dichloromethane (250 mL) was added and the solution was charged to a separatory funnel. The organic layer was washed twice with water and brine and dried over MgSO4. Filtration and concentration in vacuo afforded 28 as a yellow foam. Wt.: 15.1 g (90%). 1H NMR (300 MHz, CDCl3) δ 8.62 (d, 1H), 8.26 (m, 2H), 7.69 (m, 2H), 7.20 (m, 1H), 4.92 (d, 1H), 3.82 (m, 2H), 3.26 (m, 1H), 2.70 (m, 2H), 1.61 (m, 2H), 1.40 (s, 9H), 1.24 (m, 2H); LC/MS m/z 409 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329755B2
Source datasetuspto-grants-2008_02
ORD IDord-097f9c4d7f49413087641f55171733ac
Source noteuspto-grants-2008_02