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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540773Generated: October 29, 2026

Tetrahydrofurfurylamine → HCID 52914351, compound

https://huagongshe.com/reaction/540773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofurfurylamineHCID 253298—
ReactantHCID 52913937HCID 52913937—
SolventDimethylformamideHCID 6228—
ProductHCID 52914351HCID 52914351—

Reaction Conditions

Temperature22 °C

Reaction Steps

1-(tetrahydrofuran-2-yl)methanamine (12.3 mgs, 0.121 mmol, 1.2 equiv) followed by Si-bound cyanoborohydride (322 mg, 0.303 mmol, 3.0 equiv, 0.94 mmol/g) were added to N-(2-{3-[1-ethyl-5-(4-formylphenoxy)-1H-pyrazol-3-yl]phenyl}propan-2-yl)-2,2,2-trifluoroethanesulfonamide (50.0 mg, 0.101 mmol, 1 equiv) stirring in DMF (with 0.05% acetic acid v:v, 0.5 mL). The resulting mixture was stirred at 22° C. for 16 hours then filtered through a 0.45 micron nylon syringe filter and flushed with methanol. The filtrate was purified by reversed phase HPLC (0-95% acetonitrile:water with 0.025% TFA v:v). Pure fractions were identified, combined, basified with saturated aqueous sodium bicarbonate and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. The drying agent was filtered away and the filtrate was concentrated in vacuo to give N-(2-{3-[1-ethyl-5-(4-{[(tetrahydrofuran-2-ylmethyl)amino]methyl}phenoxy)-1H-pyrazol-3-yl]phenyl}propan-2-yl)-2,2,2-trifluoroethanesulfonamide. Calc'd (M+1) 581.2. Found: 581.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871796B2
Source datasetuspto-grants-2014_10
ORD IDord-3611655998404d96bf508fb5810efe9f
Source noteuspto-grants-2014_10