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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479837Generated: October 30, 2026

Diethyl Pyrocarbonate → N-[[2,6-bis[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]-2-[(4-chlorophenyl)sulfonyl-ethyl-amino]prop-2-enamide

https://huagongshe.com/reaction/1479837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl PyrocarbonateHCID 3051—
Reactant[2,6-Bis[4-(trifluoromethyl)phenyl]-4-pyridyl]methanamineHCID 90384398—
Reactant2-[(4-Chlorophenyl)sulfonyl-ethyl-amino]prop-2-enoic acidHCID 131736586—
SolventTetrahydrofuranHCID 8028—
ProductN-[[2,6-bis[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]-2-[(4-chlorophenyl)sulfonyl-ethyl-amino]prop-2-enamideHCID 9038416221%

Reaction Steps

Acid 4D (289.74 mg, 1 mmol) was dissolved in 10 ml of THF and at rt DEPC (1.1 equiv, 0.15 ml) and [2,6-bis[4-(trifluoromethyl)phenyl]-4-pyridyl]methanamine 29A (1.1 equiv., 400 mg) were added to the solution. The mixture was stirred at rt overnight then evaporated. The residue 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 by chromatographic column (3:7 EtOAc:petroleum ether) afforded 140 mg of a white solid. Yield=21% 1HNMR (DMSO, 400 MHz) δ 1.25 (3H, t), 3.40 (2H, q), 4.60 (2H, d), 5.18 (1H, s), 6.18 (1H, s), 7.70 (2H, d), 7.82 (2H, d), 7.86 (4H, d), 8.02 (2H, s), 8.40 (4H, d), 8.89 (1H, bt) [M+1] 668.9 (C31H24ClF6N3O3S requires 668.05).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409864B2
Source datasetuspto-grants-2016_08
ORD IDord-16b63bb9faef4defa55876e3264acd4b
Source noteuspto-grants-2016_08