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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921108Generated: November 4, 2026

Triethylamine → Ethyl (2S)-2-(tert-butoxy)-2-[4,23-dimethyl-16-(trifluoromethyl)-11,22-dioxa-1,5,7,8-tetraazapentacyclo[21.2.2.16,9.02,7.013,18]octacosa-2,4,6(28),8,13(18),14,16,19-octaen-3-yl]acetate

https://huagongshe.com/reaction/921108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
Reactant(S)-Ethyl 2-(7-(4-(allyloxy)-4-methylpiperidin-1-yl)-2-(((2-bromo-4-(trifluoromethyl)benzyl)oxy)methyl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-(tert-butoxy)acetateHCID 118321378—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventAcetonitrileHCID 6342—
ProductEthyl (2S)-2-(tert-butoxy)-2-[4,23-dimethyl-16-(trifluoromethyl)-11,22-dioxa-1,5,7,8-tetraazapentacyclo[21.2.2.16,9.02,7.013,18]octacosa-2,4,6(28),8,13(18),14,16,19-octaen-3-yl]acetateHCID 13173490463%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a pressure tube flushed with N2 were added (S)-ethyl 2-(7-(4-(allyloxy)-4-methylpiperidin-1-yl)-2-(((2-bromo-4-(trifluoromethyl)benzyl)oxy)methyl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-(tert-butoxy)acetate (0.200 g, 0.281 mmol), acetonitrile (8 ml) and triethylamine (0.392 ml, 2.81 mmol). Added to this solution were triphenylphosphine (0.022 g, 0.084 mmol) and tris(dibenzylideneacetone)dipalladium (0) (0.026 g, 0.028 mmol). The tube was sealed and stirred at 120° C. for 23 h. The mixture was cooled, filtered and concentrated to give a yellow residue that was purified by flash chromatography (Biotage; 0%-100% EtOAc/hexane; 20 CV) to give the title compound (0.1115 g, 0.177 mmol, 62.9% yield) as a yellow foam. LCMS (M+H) calcd for C34H44F3N4O4: 631.31. found: 631.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273067B2
Source datasetuspto-grants-2016_03
ORD IDord-8345eb48d8fd4177a6b9184c63289342
Source noteuspto-grants-2016_03