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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-amineHCID 64173296—
ReactantEthyl 4-(4,4,4-trifluorobutanoyl)benzoateHCID 68157804—
ReactantHCID 178419135HCID 178419135—
SolventMethanolHCID 887—
ProductHCID 86669093HCID 8666909343,921%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859591B2
Source datasetuspto-grants-2014_10
ORD IDord-304f88c2c96d4a44bb52e52e43e262b6
Source noteuspto-grants-2014_10