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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410353Generated: November 4, 2026

Cyclopentanemethanol → tert-Butyl 4-({[4-(cyclopentylmethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2410353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanemethanolHCID 77195—
ReactantMethyl 1-{[4-(hydroxymethyl)piperidin-1-yl]methyl}cyclopentanecarboxylateHCID 69317059—
ReactantHCID 136263840HCID 136263840—
Producttert-Butyl 4-({[4-(cyclopentylmethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidine-1-carboxylateHCID 69317710—

Reaction Steps

The title compound was prepared according to the procedure described in Step 4 of EXAMPLE 9 using tert-butyl 4-{[(4-hydroxy-1,2-benzisoxazol-3-yl)oxy]methyl}piperidine-1-carboxylate (EXAMPLE 17, Step 2) and cyclopentylmethanol instead of 4-[(4-methoxybenzyl)oxy]-1,2-benzisoxazol-3-ol and methyl 1-{[4-(hydroxymethyl)piperidin-1-yl]methyl}cyclopentanecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816090B2
Source datasetuspto-grants-2014_08
ORD IDord-86a35938e8ad48fa9f005cdb6e27051e
Source noteuspto-grants-2014_08