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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607096Generated: November 1, 2026

4-Benzylpiperidine → HCID 19851863, compound

https://huagongshe.com/reaction/1607096

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BenzylpiperidineHCID 31738—
ReactantHCID 15616513HCID 15616513—
ProductHCID 19851863HCID 19851863—

Reaction Steps

N-triphenylmethyl-2-paranitrophenoxycarbonylthioethylamine (300 mg) and 4-benzylpiperidine (327 μl) were subjected to similar reactions to those described in References 2 and 4 to give 2-(4-benzylpiperidino)carbonylthioethylamine (crude formate: 210 mg). The product was dissolved in anhydrous methanol (3.5 ml). Triethylamine (432 μl) and mitocyin A (151 mg: 0.7 molar equivalent) were added to the solution which was then treated in a similar manner to that described in Example 1 to obtain Compound 41 (300 mg) in the form of grayish blue powders with a yield of 81%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863935
Source datasetuspto-grants-1989_09
ORD IDord-468c56c5070f4da0a621efaf7000d5a4
Source noteuspto-grants-1989_09