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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485874Generated: October 30, 2026

HCID 59242670, compound → HCID 59242651, compound

https://huagongshe.com/reaction/1485874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59242670HCID 59242670—
SolventMethanolHCID 887—
ProductHCID 59242651HCID 59242651—

Reaction Steps

To a solution of 4-[5-(5-chloro-thiophen-2-yl)-6-trifluoromethyl-pyridazin-3-yl]-piperazine-1-carboxylic acid tert-butyl ester (D15) (0.114 g, 0.25 mmol) in methanol (10 ml) was added Amberlyst® 15 ion exchange resin, acidic form (4.1 mmol/g) (0.305 g, 1.25 mmol) and the reaction mixture was shaken at room temperature for 18 h. After this period, the mixture was filtered and then a saturated solution of ammonia in methanol was added. The mixture was shaken for 1 h, filtered and the filtrate evaporated in vacuo. The residue was then purified by column chromatography (silica gel; 3% ammonia in methanol (7M)/dichloromethane). The desired fractions were collected and evaporated in vacuo. The crude product was dissolved in a 2 M solution of hydrochoric acid in diethyl ether and the mixture stirred at room temperature for 16. The solvent was evaporated in vacuo. The solid obtained was triturated from diethyl ether to yield E27 (0.062 g, 87%). C13H12ClF3N4S requires 348; Found 349 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422296B2
Source datasetuspto-grants-2016_08
ORD IDord-f32c5ef934484969b864ed950d1e88d6
Source noteuspto-grants-2016_08