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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470767Generated: October 31, 2026

2-Methyltetrahydrofuran → N-((1S)-1-(4-(1-(4-((2-methylcyclopropyl)methoxy)phenyl)-piperidin-4-yl)phenyl)ethyl)acetamide

https://huagongshe.com/reaction/1470767

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethyltetrahydrofuranHCID 7301—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(2-Methylcyclopropyl)methanolHCID 138655—
Reactant(S)-N-{1-(4-[1-(4-Hydroxyphenyl)-piperidin-4-yl]-phenyl}-ethyl)-acetamideHCID 67125424—
ProductN-((1S)-1-(4-(1-(4-((2-methylcyclopropyl)methoxy)phenyl)-piperidin-4-yl)phenyl)ethyl)acetamideHCID 67970640—

Reaction Steps

50 mg (0.15 mmol) (S)—N-{1-(4-[1-(4-Hydroxyphenyl)-piperidin-4-yl]-phenyl}-ethyl)-acetamide (compound 1.48), 14 mg (0.16 mmol) 2-methylcyclopropanemethanol and 38.8 mg (0.15 mmol) triphenylphosphine are added to 2 mL 2-methyl-tetrahydrofurane at 0° C. 30.5 μl (0.15 mmol) di-iso-propyl azodicarboxylate are added and the mixture is allowed to warm to rt. Stirring is continued over night followed by addition of 0.5 equivalents of triphenylphosphine and 0.5 equivalents of di-iso-propyl azodicarboxylate. Stirring is continued for one day and again additional triphenylphosphine and di-iso-propyl azodicarboxylate are added and stirring is continued for 16 h at 50° C. Then the mixture is filtered and purified using reversed phase HPLC (water/MeOH, 0.1% FA) to yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006450B2
Source datasetuspto-grants-2015_04
ORD IDord-a9b1195a2a894575b84b9977b7961a82
Source noteuspto-grants-2015_04