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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (2-Amino-5-methyl-4-trifluoromethyl-phenyl)-carbamic acid tert-butyl ester | HCID 67361461 | — |
| Reactant | HCID 69688870 | HCID 69688870 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18548894 | HCID 18548894 | 37.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06548495B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-b6b2e955bb824932b9625666926c8fb3 |
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| Source note | uspto-grants-2003_04 |
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