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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920809Generated: October 29, 2026

Tetrahydrofuran → HCID 118061901, compound

https://huagongshe.com/reaction/920809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant3,3-Difluorocyclopentane-1-carboxylic acidHCID 53403837—
Reactant2-(3-Chloro-4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine-3-carboxamideHCID 118061627—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 118061901HCID 118061901—

Reaction Conditions

Temperature70 °C

Reaction Steps

A stirred solution of Intermediate 332C (32.6 mg, 0.217 mmol) in toluene (1 mL) at RT under nitrogen was added with TEA (0.045 mL, 0.325 mmol) and DPPA (0.050 mL, 0.217 mmol) and heated to 70° C. for 2 h. The reaction mass was cooled to RT and to it was added a solution of Intermediate 185B (30 mg, 0.108 mmol) in THF (1 mL) and stirred at RT for 16 h. The reaction mass was diluted with ethyl acetate (25 mL), washed with water and brine, dried over anhydrous Na2SO4, filtered, and the filtrate concentrated under reduced pressure. The individual isomers were separated by preparative chiral SFC (Column: WHELK-O® 1 (R,R) (250×4.6 mm), 5μ column, 5 Co-Solvent: 0.2% DEA, Column Temperature: 24.4, Total Flow: 3 mL, CO2 Flow Rate: 2.1, Co-Solvent Flow Rate: 0.9, Co-Solvent %: 30%, Back Pressure: 101 bar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273058B2
Source datasetuspto-grants-2016_03
ORD IDord-14f80af829e246b6a911eefc35597fd8
Source noteuspto-grants-2016_03