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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196540Generated: October 30, 2026

Potassium Carbonate → HCID 59843243, compound

https://huagongshe.com/reaction/2196540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactanttert-Butyl (3S)-3-bromopyrrolidine-1-carboxylateHCID 34179480—
Reactant4-(5-(furan-2-yl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)thiophene-2-carbonitrileHCID 59843204—
ReactantHCID 178506075HCID 178506075—
SolventDimethylformamideHCID 6228—
ProductHCID 59843243HCID 5984324337%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 72 (681 mg, 2.72 mmol) in DMF (9.894 mL) was added potassium carbonate (855 mg, 6.18 mmol), and then 5-(furan-2-yl)-3-(trifluoromethyl)-1H-pyrazole (500 mg, 2.474 mmol) [made by following the procedure described above for the synthesis of compound 14 (scheme 2, example 1c, step 4), except using hydrazine hydrate instead of 13 as the starting material]. The resulting solution was allowed to stir at 100° C. for 1 h. The mixture was quenched with water and extracted with ethyl acetate, washed with brine, dried (MgSO4) filtered and concentrated. The residue was purified by silica gel column chromatography with gradient of EtOAc (10-20%) in hexanes to afford 73 (340 mg, 37%) as a colorless oil. LRMS (ESI): calc. 371.1; found 394.0 (MNa)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338437B2
Source datasetuspto-grants-2012_12
ORD IDord-342666d769de4839a007dbf02e282d1a
Source noteuspto-grants-2012_12