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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383380Generated: October 31, 2026

Di-tert-butyl (9-bromononyl)imidodicarbonate → Di-tert-butyl{9-[4-({3-[cyclohexyl(hydroxy)phenylmethyl]-1H-1,2,4-triazol-1-yl}methyl)-piperidin-1-yl]nonyl}imidodicarbonate

https://huagongshe.com/reaction/2383380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl (9-bromononyl)imidodicarbonateHCID 21880675—
Reactantcyclohexyl(phenyl)[1-(piperidin-4-ylmethyl)-1H-1,2,4-triazol-3-yl]methanolHCID 59145970—
ProductDi-tert-butyl{9-[4-({3-[cyclohexyl(hydroxy)phenylmethyl]-1H-1,2,4-triazol-1-yl}methyl)-piperidin-1-yl]nonyl}imidodicarbonateHCID 5914595061%

Reaction Steps

The title compound was prepared from cyclohexyl(phenyl)[1-(piperidin-4-ylmethyl)-1H-1,2,4-triazol-3-yl]methanol (Preparation 20, 300 mg, 0.846 mmol) and di-tert-butyl (9-bromononyl)imidodicarbonate (U.S. Pat. No. 4,167,167, 357 mg, 0.846 mmol) using the same method as described in preparation 5, to give a white foam, in 61% yield, 360 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263623B2
Source datasetuspto-grants-2012_09
ORD IDord-e5ee393a3f9840fab8af237e472ab31e
Source noteuspto-grants-2012_09