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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949074Generated: October 31, 2026

Triethylamine → Acetic acid 1-benzyl-4-[methyl-(4-trifluoromethoxy-phenyl)-carbamoyl]-piperidin-4-yl ester

https://huagongshe.com/reaction/1949074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiisopropylethylamineHCID 81531—
ReactantPotassium bisulfateHCID 516920—
Reactantn-Methyl-4-(trifluoromethoxy)anilineHCID 737351—
Reactant4-(Acetyloxy)-1-benzylpiperidine-4-carboxylic acidHCID 53302252—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductAcetic acid 1-benzyl-4-[methyl-(4-trifluoromethoxy-phenyl)-carbamoyl]-piperidin-4-yl esterHCID 5812932972%

Reaction Steps

A mixture of 1.4 g (5 mmol) 4-acetoxy-1-benzyl-piperidine-4-carboxylic acid 0.49 mL (5.8 mmol) oxalylchloride, cat. amount DMF and 2.1 mL (15 mmol) NEt3 in DCM at 0° C. was stirred for 1 h. The mixture was concentrated and to 0.79 g (2.42 mmol) of the acid chloride and 2.1 mL (12.1 mmol) DIPEA in 25 mL DCM was added 0.554 g (2.9 mmol) methyl-(4-trifluoromethoxy-phenyl)-amine. The mixture was stirred for 15 h at room temperature. KHSO4 (1N) was added and the mixture was extracted with DCM. The combined organic extracts were dried with MgSO4 and evaporated. 0.782 g (72%) of the title compounds as obtained. MS (m/e): 451.3 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399676B2
Source datasetuspto-grants-2013_03
ORD IDord-feddd21363f24556bcb0256c0d248376
Source noteuspto-grants-2013_03