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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858758Generated: October 31, 2026

HCID 13524712, compound → HCID 86604467, compound

https://huagongshe.com/reaction/1858758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13524712HCID 13524712—
ReactantHCID 86604468HCID 86604468—
SolventDichloromethaneHCID 6344—
ProductHCID 86604467HCID 86604467—

Reaction Steps

In an analogous manner to that described in Example 74(f), from tert-butyl (3RS,4RS,5SR)-4-[4-(3-benzyloxy-propoxy)-phenyl]-3-hydroxymethyl-5-(2-morpholin4-yl-ethoxymethyl)-piperidine-1-carboxylate by oxidation with dimethyl sulphoxide/oxalyl chloride in methylene chloride there was obtained tert-butyl (3RS,4SR,5SR)-4-[4-(3-benzyloxy-propoxy)-phenyl]-3-formyl-5-(2-morpholin-4-yl-ethoxymethyl)-piperidine-1-carboxylate as a yellow oil; MS: 597 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150526
Source datasetuspto-grants-2000_11
ORD IDord-809f20d2ab5d4879b793689bb613864c
Source noteuspto-grants-2000_11