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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266898Generated: November 4, 2026

(2-Amino-5-methyl-4-trifluoromethyl-phenyl)-carbamic acid tert-butyl ester → HCID 18548894, compound

https://huagongshe.com/reaction/1266898

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Amino-5-methyl-4-trifluoromethyl-phenyl)-carbamic acid tert-butyl esterHCID 67361461—
ReactantHCID 69688870HCID 69688870—
SolventTolueneHCID 1140—
ProductHCID 18548894HCID 1854889437.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (2-amino-5-methyl-4-trifluoromethyl-phenyl)-carbamic acid tert-butyl ester (Example J15) (0.145 g) and 3-[3-[5-methyl-2-(tetrahydro-pyran-2-yloxymethyl)-thiazol-4-yl]-phenyl]-3-oxo-propionic acid tert.-butyl ester (Example K18) (0.18 g) in toluene (1.5 mL) was heated to 100° C. for 8 h. The mixture was cooled and evaporated in vacuum. A solution of the residue in a mixture of CH2Cl2 (2.5 mL) and trifluoroacetic acid (2.5 mL) was stirred for 0.5 h at 20° C. The mixture was evaporated in vacuum, the residual oil was dissolved in AcOEt and the solution was washed with saturated NaHCO3 solution and with brine, dried over Na2SO4 and evaporated in vacuum. The residue was triturated with CH2Cl2 to give the title compound (0.07 g) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548495B2
Source datasetuspto-grants-2003_04
ORD IDord-b6b2e955bb824932b9625666926c8fb3
Source noteuspto-grants-2003_04