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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752014Generated: October 28, 2026

Hydrochloride methanol → HCID 67255827, compound

https://huagongshe.com/reaction/1752014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
ReactantHCID 67256764HCID 67256764—
SolventMethanolHCID 887—
ProductHCID 67255827HCID 67255827—

Reaction Steps

5-(4-Chlorobenzyl)-2-methoxymethoxymethyl-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol (Compound (VII), R1=CH3, Ym=4-Cl, G=CH2OCH3, A=N) (629 mg, 1.66 mmol) was dissolved in methanol (6.3 ml), 10% hydrogen chloride-methanol (6.3 ml, 1.73 mmol) was added and stirring was conducted at room temperature for 48 hours. After completion of the reaction, the solvent was distilled away, and water was added. After ethyl acetate (80 ml) was added, an aqueous solution of sodium hydroxide was added until the pH became 10. The organic layer was separated, washed with saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled away to obtain the title compound (VI-1 (Compound (VI), (Ra2)Xa2na2(OH)pa1=CH3, (Rb2)Xb2nb2(OH)pb1=CH2OH, Ym=4-Cl, A=N, isomer type: C): VI-2 (Compound (VI), (Ra2)Xa2na2(OH)pa1=CH2OH, (Rb2)Xb2nb2(OH)pb1=CH3, Ym=4-Cl, A=N, isomer type: C): other isomers (isomer type: T)=6:3:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162966B2
Source datasetuspto-grants-2015_10
ORD IDord-1f1aea0b9a4e4ed1b1e2519d248c4c0c
Source noteuspto-grants-2015_10