HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537574Generated: October 29, 2026
6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-amine → HCID 86669093, compound
https://huagongshe.com/reaction/537574
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-amine | HCID 64173296 | — |
| Reactant | Ethyl 4-(4,4,4-trifluorobutanoyl)benzoate | HCID 68157804 | — |
| Reactant | HCID 178419135 | HCID 178419135 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86669093 | HCID 86669093 | 43,921% |
Reaction Steps
To a solution of crude ethyl 4-(4,4,4-trifluorobutanoyl)benzoate (0.060 g, 0.22 mmol) and 6-[4-(trifluoromethyl)-1H-pyrazol-1-yl]pyridin-3-amine (0.050 g, 0.22 mmol) in methanol (2.2 ml) was added decaborane (8.0 mg, 0.066 mmol). The reaction was stirred for 12 hours at ambient temperature. The reaction mixture was quenched with aqueous 1.0M hydrochloric acid and concentrated in vacuo. The crude material was purified via ISCO MPLC (SiO2, 0-100% ethyl acetate in heptane) to yield the product (47 g, 42%) as an oil. 1H NMR (400 MHz, CDCl3): δ 8.63 (s, 1H), 8.06 (d, J=8.4 Hz, 2H), 7.80 (s, 1H), 7.75 (d, J=2.5 Hz, 1H), 7.70 (d, J=8.8 Hz, 1H), 7.38-7.45 (m, 2H), 6.96 (dd, J=8.8, 2.7 Hz, 1H), 4.50 (t, J=6.2 Hz, 1H), 4.37 (q, J=7.0 Hz, 2H), 2.07-2.32 (m, 4H), 1.39 (t, J=7.2 Hz, 3H). MS (M+1): 487.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08859591B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-304f88c2c96d4a44bb52e52e43e262b6 |
|---|
| Source note | uspto-grants-2014_10 |
|---|