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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200083Generated: October 31, 2026

Diisopropylethylamine → HCID 76072182, compound

https://huagongshe.com/reaction/2200083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 1259362HCID 1259362—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 62648620HCID 62648620—
SolventDichloromethaneHCID 6344—
ProductHCID 76072182HCID 7607218218%

Reaction Steps

A solution of crude [1-(4-trifluoromethyl-phenyl)-piperidin-3-yl]-methylamine (30.0 mg, 0.12 mmol, crude) and [ethyl-(4-fluoro-benzenesulfonyl)-amino]-acetic acid (30.0 mg, 0.12 mmol) in dichloromethane (5 mL) at 25° C. was treated with HATU (43.7 mg, 0.12 mmol). N,N-Diisopropylethylamine (29.7 mg, 0.23 mmol) was added to the solution. The reaction mixture was stirred for 2 h. The reaction mixture was then poured into 0.2 M aqueous KHSO4 solution and extracted three times with ethyl acetate. The combined organic layers were washed three times with water and once with brine. The organic layer was then dried over magnesium sulfate, filtered and concentrated in vacuo. Flash column chromatography (50/50 hexanes/ethyl acetate) afforded 2-[ethyl-(4-fluoro-benzenesulfonyl)-amino]-N-[1-(4-trifluoromethyl-phenyl)-piperidin-3-ylmethyl]-acetamide (10.2 mg, 18%) as a white solid. [MH]+=502.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359337B2
Source datasetuspto-grants-2016_06
ORD IDord-da887bc16a194689a69d775090eaf905
Source noteuspto-grants-2016_06