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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108464Generated: October 30, 2026

HCID 86598679, compound → HCID 11477911, compound

https://huagongshe.com/reaction/2108464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86598679HCID 86598679—
ReactantHCID 178422940HCID 178422940—
ProductHCID 11477911HCID 1147791154%

Reaction Steps

Reaction of 1-[3-(2,2,2-trifluoroethoxy)-4-trifluoromethyl-phenyl]-4,4,4-trifluoro-butane-1,3-dione (191 mg, 0.5 mmol), prepared from 4-(2,2,2-trifluoroethoxy)-3-trifluoromethyl-acetophenone (synthesis: see part acetophenone derivatives) according to general procedure A, and 3-amino-4-(2-methyl-4-pyridinyl)-pyrazole [prepared from 4-cyanomethyl-2-methyl-pyridine, as described in Bioorg. Med. Chem. Lett. 12 (2002) 3537-3541] (87 mg, 0.5 mmol) according to general procedure B yielded the title compound as a yellow solid (140 mg, 54%). MS (ISP) 521.4 [(M+H)+]; mp 201° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514443B2
Source datasetuspto-grants-2009_04
ORD IDord-5c221d8fd58a4394b3e4b23a7b7545c4
Source noteuspto-grants-2009_04