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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907136Generated: October 30, 2026

Chloromethyl Methyl Ether → HCID 25175790, compound

https://huagongshe.com/reaction/1907136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantPotassium HydroxideHCID 14797—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 57990205HCID 57990205—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 25175790HCID 25175790—

Reaction Steps

A mixture of 5-chloro-6-{[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazole-3-carbonyl]-amino}-1H-indazole-7-carboxylic acid isopropylamide (1.00 g, 1.90 mmol), KOH (310 mgs, 5.70 mmol) and t-BuOK (6.4 mg, 0.02 mmol) in THF (5 mL) was treated dropwise with chloro-methoxy-methane (0.39 mL, 5.1 mmol). The resulting reaction mixture was stirred at ambient temperature for 18 h. AcOEt and water was added. The phases were separated. The aqueous layer was extracted with AcOEt. The organic layers were washed with water, combined, dried over MgSO4 and concentrated in vacuo. Purification of the residue by reverse phase HPLC affords the title product as a colorless solid. M.p. 180-182° C., LC/MS: 570/572 (M+H)+, 592/594 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598078B2
Source datasetuspto-grants-2013_12
ORD IDord-ee44c8c82b5e454185d02de4b544952e
Source noteuspto-grants-2013_12