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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712419Generated: October 31, 2026

Hydrochloric Acid → HCID 86610004, compound

https://huagongshe.com/reaction/1712419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 86610005HCID 86610005—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86610004HCID 86610004—

Reaction Conditions

Temperature-40 °C

Reaction Steps

4.8 ml of diisobutylaluminium hydride (1.5M in toluene) are added dropwise at −70° C. over 10 minutes to the solution of 1.74 g of tert-butyl 3-[2-(6-chloro-5-methoxycarbonylmethyl-2-methylpyrimidin-4-yloxy)ethoxy]-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate in 20 ml of tetrahydrofuran. The reaction mixture is warmed slowly to −40° C. over 3 hours, admixed with 0.4 ml of methanol and subsequently warmed to room temperature. The reaction solution is admixed with 20 ml of 0.5N HCl and stirred vigorously over 10 minutes. The reaction mixture is extracted with tert-butyl methyl ether (2×). The combined organic phases are washed successively with 1M sodium potassium tartrate solution and brine, dried over sodium sulphate and concentrated by evaporation. The title compound is obtained as a colourless oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.35 (2:1 EtOAc-heptane); Rt=5.75.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790715B2
Source datasetuspto-grants-2010_09
ORD IDord-3fa83050af96482eb63de6c2de7425f5
Source noteuspto-grants-2010_09