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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200084Generated: November 1, 2026

Diisopropylethylamine → HCID 76072183, compound

https://huagongshe.com/reaction/2200084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPotassium bisulfateHCID 516920—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-[N-(propan-2-yl)4-fluorobenzenesulfonamido]acetic acidHCID 60827977—
ReactantHCID 62648620HCID 62648620—
SolventDichloromethaneHCID 6344—
ProductHCID 76072183HCID 7607218353.9%

Reaction Steps

A solution of crude [1-(4-trifluoromethyl-phenyl)-piperidin-3-yl]-methylamine (47.0 mg, 0.18 mmol, crude) and [(4-fluoro-benzenesulfonyl)-isopropyl-amino]-acetic acid (50.0 mg, 0.18 mmol) in dichloromethane (5 mL) at 25° C. was treated with HATU (69.1 mg, 0.18 mmol). N,N-Diisopropylethylamine (46.9 mg, 0.36 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 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-[(4-fluoro-benzenesulfonyl)-isopropyl-amino]-N-[1-(4-trifluoromethyl-phenyl)-piperidin-3-ylmethyl]-acetamide (50.0 mg, 53%) as a white solid. [MH]+=516.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359337B2
Source datasetuspto-grants-2016_06
ORD IDord-ac7c00736f2c44df92cabf657e5ee972
Source noteuspto-grants-2016_06