HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099283Generated: October 31, 2026
Ethanamine, 2,2,2-trifluoro- → HCID 59404973, compound
https://huagongshe.com/reaction/1099283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanamine, 2,2,2-trifluoro- | HCID 9773 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 59232186 | HCID 59232186 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 59404973 | HCID 59404973 | 36.4% |
Reaction Steps
To a suspension of N-[4-(4-amino-7-formylpyrrolo[2,1-f][1,2,4]triazin-5-yl)phenyl]-N′-[6-(trifluoromethyl)pyridin-2-yl]urea (5.0 mg, 0.011 mmol) in 1,2-dichloroethane (2 mL) was added 2,2,2-trifluoroethylamine (11.2 mg, 0.11 mmol), followed by sodium triacetoxyborohydride (24.0 mg, 0.11 mg). The mixture was stirred at rt under nitrogen for 4 d. The solvent was evaporated under reduced pressure. The residue was dissolved in DMF and purified by HPLC using a gradient of 20-90% MeCN in water to yield 2.1 mg (35%) of the title compound. 1H-NMR (DMSO-d6) 9.95 (bs, 1 H), 9.79 (bs, 1 H), 8.05-7.99 (m, 2 H), 7.90 (s, 1 H), 7.57 (d, J=8.6, 2 H), 7.50 (dd, J=6.4, 1.7, Hz, 1 H), 7.40 (d, J=8.6 Hz, 2 H), 6.66 (s, 1 H), 4.07 (d, J=6.8 Hz, 2 H), 3.30-3.23 (m, 2 H), 2.92-2.85 (m, 1 H); MS [M+H]+=525.1; LCMS RT=2.91 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143393B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-aca4cfe25f9f4be9a939826057b75121 |
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| Source note | uspto-grants-2012_03 |
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