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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16597Generated: October 25, 2026

tert-butyl N-((4-hydroxypiperidin-4-yl)methyl)carbamate → Methyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}-4-hydroxypiperidine-1-yl)methyl]cyclohexanecarboxylate

https://huagongshe.com/reaction/16597

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-((4-hydroxypiperidin-4-yl)methyl)carbamateHCID 10868112—
ReactantMethyl 1-(iodomethyl)cyclohexanecarboxylateHCID 58947958—
ProductMethyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}-4-hydroxypiperidine-1-yl)methyl]cyclohexanecarboxylateHCID 68584740—

Reaction Steps

The title compound was prepared by a method similar to that shown in the Step 2 of Example 3 by using tert-butyl [(4-hydroxypiperidin-4-yl)methyl]carbamate (Chem. Pharm. Bull., 2002, 50 (9) 1187-1194) and methyl 1-(iodomethyl)cyclohexanecarboxylate (Step 1 of Example 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737163B2
Source datasetuspto-grants-2010_06
ORD IDord-f421c7f7466e48a39f178fd0a01ee711
Source noteuspto-grants-2010_06