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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358393Generated: November 1, 2026

Diethyl Pyrocarbonate → 3-(4-Tert-butylphenyl)propynoic acid 3-fluoro-4-methanesulfonylamino-5-vinylbenzylamide

https://huagongshe.com/reaction/2358393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl PyrocarbonateHCID 3051—
Reactant3-(4-tert-butylphenyl)prop-2-ynoic AcidHCID 11344701—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 57665528HCID 57665528—
SolventDimethylformamideHCID 6228—
Product3-(4-Tert-butylphenyl)propynoic acid 3-fluoro-4-methanesulfonylamino-5-vinylbenzylamideHCID 1185257772.25%

Reaction Steps

A mixture of (4-tert-Butylphenyl)propynoic acid (step 2 of Example 11, 0.16 mmol, 33.0 mg) and N-(4-aminomethyl-2-fluoro-6-vinylphenyl)methanesulfonamide (step 6 of Example 2, 0.19 mmol, 39.20 mg), DEPC (1.2 eq, 0.19 mmol, 29.13 μl), TEA (2 eq, 0.32 mmol, 44.60 μl) in DMF under an Ar atmosphere was stirred at room temperature for 12 h. Upon completion, as determined by TLC, the reaction solution was extracted by EtOAc (150 ml×3) and the organic phase was washed with H2O, dried (Na2SO4), filtered and concentrated. After silica gel column chromatography (n-hexane/EtOAc=2:1), 3-(4-tert-butylphenyl)propynoic acid 3-fluoro-4-methanesulfonylamino-5-vinylbenzylamide (49.5 mg, 0.11 mmol, 72.25%) was isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763657B2
Source datasetuspto-grants-2010_07
ORD IDord-46f2487ff0b1475e932a749834102d01
Source noteuspto-grants-2010_07