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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414910Generated: October 31, 2026

Methanol → HCID 23512960, compound

https://huagongshe.com/reaction/2414910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPhenethylamineHCID 1001—
Reactant1-Methyl-4-piperidoneHCID 74049—
ReactantHCID 3153429HCID 3153429—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 23512960HCID 23512960—

Reaction Steps

4-Alpha-methylbenzylamino-1-methyl-piperidine (47AKU-36) DL-Phenylethylamine (606 mg, 5.0 mmol) was dissolved in 10 ml methanol and 1-Methyl-4-piperidone (566 mg, 5.0 mmol) in 10 ml methanol was added. Mixture was stirred and Acetic acid (˜0.75 ml) was added until pH˜5. NaCNBH3 (628 g, 10 mmol) was slowly added. Gas evolution observed. After magnetic stirring for 20 hrs methanol was partly removed on Rotavapor (40° C.). Ethylacetate, 2M NaOH and water were added until pH˜10. Phases were separated and aq. phase was then re-extracted with ethylacetate and dichloromethane. Combined organic phases were dried over MgSO4. Concentration on Rotavapor (40° C.) yielded 838 mg crude 47AKU-36. TLC (10% methanol in dichloromethane): Rf=0.3. HPLC-MS (Method A): M+=219.1 (UV/MS(%)=100/94).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06815458B2
Source datasetuspto-grants-2004_11
ORD IDord-8f2b741c33f2406e95bcbec3d981ca9a
Source noteuspto-grants-2004_11