Piperidine → HCID 18397572, compound

HRID 1387028Notes

Reaction equation

[CH:1]12[O:6][CH:2]1[CH2:3][CH2:4][CH2:5]2.[NH:7]1[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1>>[N:7]1([C@@H:2]2[CH2:3][CH2:4][CH2:5][C@H:1]2[OH:6])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1

Participants

Reactant 2

HCID 8082Piperidine

HCID 92446-Oxabicyclo[3.1.0]hexane

Product 1

HCID 18397572HCID 18397572, compoundYield 81%

Procedure

The title compound was prepared in 81% yield from cyclopentene oxide and piperidine by essentially following the procedures outlined in Example 20, Part A.

Sources & evidence

ORD record: ord-18c2864109734692a09e44756dda5998
Source dataset: uspto-grants-2001_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06265575B1

Reaction notes

Loading…