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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624772Generated: October 27, 2026

Tris(furan-2-yl)phosphane → HCID 67216572, compound

https://huagongshe.com/reaction/624772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(furan-2-yl)phosphaneHCID 521585—
Reactant3-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride)HCID 2734385—
ReactantHCID 67216767HCID 67216767—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystCuprous 2-thiophenecarboxylateHCID 11194830—
ProductHCID 67216572HCID 6721657285.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

Note: THF was degassed with a stream of N2 for 10 min. in a separate flask. Tert-butyl cyclopropyl(2-(methylthio)pyrazolo[1,5-a][1,3,5]triazin-4-yl)carbamate (100 mg, 0.31 mmol), 3-(trifluoromethoxy)phenyl boronic acid (154 mg, 0.74 mmol), tri(2-furyl)phosphine (86 mg, 0.37 mmol), copper(I) thiophene-2-carboxylate (167 mg, 0.88 mmol), Pd2dba3 (24 mg, 0.03 mmol) were combined. The flask was evacuated and backfilled with N2. THF (3.7 mL) was added and the reaction was heated to 50° C. for 5 d. The solution was diluted with Et2O (40 mL) and washed with 10% NH4OH (3×30 mL). The organic layer was dried over MgSO4, filtered and concentrated in vacuo. The solid residue was triturated with Et2O and filtered. The filtrate was concentrated in vacuo and purified via flash column chromatography (2.5-5% EtOAc/hexanes) to afford tert-butyl cyclopropyl(2-(3-(trifluoromethoxy)phenyl)pyrazolo[1,5-a][1,3,5]triazin-4-yl)carbamate (116 mg, 85%). LCMS (ES): >95% pure, m/z 436 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303033B2
Source datasetuspto-grants-2016_04
ORD IDord-9b233a5446a74ce797a1788184137f3e
Source noteuspto-grants-2016_04