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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266897Generated: November 2, 2026

Trifluoroacetic acid → HCID 18548745, compound

https://huagongshe.com/reaction/1266897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(2-Amino-4-pyrrol-1-yl-phenyl)-carbamic acid tert-butyl esterHCID 69488996—
Reactant3-(2-Cyano-pyridin-4-yl)-3-oxo-propionic acid tert-butyl esterHCID 69592816—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 18548745HCID 1854874535.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (2-amino-4-pyrrol-1-yl-phenyl)-carbamic acid tert-butyl ester (Example J2) (0.14 g) and 3-(2-cyano-pyridin-4-yl)-3-oxo-propionic acid tert-butyl ester (Example K3) (0.14 g) in toluene (1.5 mL) was heated to 100° C. for 4 h, a fine precipitate being formed. The mixture was cooled and the precipitae was isolated by filtration. A solution of this solid in CH2Cl2 (2.5 mL) and TFA (2.5 mL) was stirred for 0.5 h at 20° C. and then evaporated in vacuum. The residual oil was dissolved in AcOEt and the solution was washed with saturated Na2CO3 solution and with brine, dried over Na2SO4 and evaporated in vacuum. The solid residue was triturated with CH2Cl2 to give the title compound (0.06 g) as light-yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548495B2
Source datasetuspto-grants-2003_04
ORD IDord-c12761b58c5747db91a8c8048380bf43
Source noteuspto-grants-2003_04