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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505203Generated: November 2, 2026

Diethyl Pyrocarbonate → N-(4-(trifluoromethyl)-2-(piperidin-1-yl)benzyl)-2,3-dihydro-2-oxobenzo[d]oxazole-4-carboxamide

https://huagongshe.com/reaction/1505203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl PyrocarbonateHCID 3051—
Reactant2-Oxo-2,3-dihydro-1,3-benzoxazole-4-carboxylic acidHCID 10921091—
Reactant(4-(Trifluoromethyl)-2-(piperidin-1-yl)phenyl)-methanamineHCID 58873623—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-(trifluoromethyl)-2-(piperidin-1-yl)benzyl)-2,3-dihydro-2-oxobenzo[d]oxazole-4-carboxamideHCID 5347693419.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

2,3-dihydro-2-oxobenzo[d]oxazole-4-carboxylic acid 21 (560 mg, 3.1 mmol) was dissolved in 20 ml of THF and at 0° C. DEPC (0.55 ml, 1.2 equiv) and amine 2c (964 mg, 1.2 equiv.) were added to the solution. The mixture was warmed at 80° C. overnight, then evaporated and the crude was dissolved in AcOEt (30 ml) and washed with water (1×20 ml) and brine. The organic phase was dried over sodium sulfate and concentrated under vacuum. The purification of the crude residue by chromatographic column using AcOEt 4/petroleum ether 6 as eluant gave 250 mg of a pale yellow solid. Yield=19% 1HNMR (DMSO, 200 MHz) δ 4.58 (2H, d, J=5.8 Hz), 7.14 (1H, t, J=8 Hz), 7.41 (4H, m), 7.68 (1H, dd, J=8 Hz, J′=0.8 Hz), 9.20 (1H, bt), 11.59 (1H, bs); [M+1] 420.2 (C21H20F3N3O3 requires 419.4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216975B2
Source datasetuspto-grants-2015_12
ORD IDord-3a51ea9d376f4d6ba0dd798276c379d9
Source noteuspto-grants-2015_12