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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349165Generated: October 30, 2026

tert-Butyl carbazate → Tert-butyl 4-[(tert-butoxycarbonyl)hydrazono]piperidine-1-carboxylate

https://huagongshe.com/reaction/349165

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl carbazateHCID 70091—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ProductTert-butyl 4-[(tert-butoxycarbonyl)hydrazono]piperidine-1-carboxylateHCID 20824233—

Reaction Steps

Reaction scheme 1 shows that the compounds of formula I can be, for example, prepared starting from 4-oxo-piperidine-1-carboxylic acid tert-butyl ester which is reacted in a first reaction step with tert-butylcarbazate to give 4-(tert-Butoxycarbonyl-hydrazono)-piperidine-1-carboxylic acid tert-butyl ester (starting compound A7). Compound A7 is reduced with, for example, the boran tetrahydrofurane complex to give 4-(N′-tert-Butoxycarbonyl-hydrazino)-piperidine-1-carboxylic acid tert-butyl ester (starting compound A6). Treatment of compound A6 with concentrated hydrochloric acid results in the formation of piperidin-4-yl-hydrazine dihydrochloride (starting compound A5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179810B2
Source datasetuspto-grants-2007_02
ORD IDord-f7392063d23c4c7c8ded5be34940ab0a
Source noteuspto-grants-2007_02