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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906638Generated: November 1, 2026

Triethylamine → N,N-Diallyl-N-({5-[(4-{3-[(trifluoromethyl)sulfonyl]anilino}piperidin-1-yl)sulfonyl]-thien-2-yl}methyl)amine

https://huagongshe.com/reaction/906638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(3-((trifluoromethyl)sulfonyl)phenyl)piperidin-4-amineHCID 2776457—
Reactant5-Diallylaminomethyl-thiophene-2-sulfonyl chlorideHCID 11380769—
SolventDichloromethaneHCID 6344—
ProductN,N-Diallyl-N-({5-[(4-{3-[(trifluoromethyl)sulfonyl]anilino}piperidin-1-yl)sulfonyl]-thien-2-yl}methyl)amineHCID 8676139886%

Reaction Steps

A solution of 4-(3-trifluoromethanesulfonyl-phenylamino)-piperidine (731 mg, 237 mmol) and Et3N (0.5 mL, 3.58 mmol) in CH2Cl2 (20 mL) was treated with the diallylamino sulfonyl chloride 269b 23° C. A thick precipitate appeared within 5 min, and the mixture was stirred overnight (even if complete within minutes). Dilution with CH2Cl2 (50 mL), washing (1120; brine), drying (MgSO4), and evaporation afforded the crude product, which was filtered over silica gel (AcOEt:cyclohexane 1:1) to afford 1.15 g (86%) of the title bisallylamine, which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012995B1
Source datasetuspto-grants-2011_09
ORD IDord-c77cbc0ec4854d71a1cc11b5f11eb2a0
Source noteuspto-grants-2011_09