HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540773Generated: October 29, 2026
Tetrahydrofurfurylamine → HCID 52914351, compound
https://huagongshe.com/reaction/540773
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofurfurylamine | HCID 253298 | — |
| Reactant | HCID 52913937 | HCID 52913937 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 52914351 | HCID 52914351 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871796B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-3611655998404d96bf508fb5810efe9f |
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| Source note | uspto-grants-2014_10 |
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