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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883165Generated: November 1, 2026

tert-Butyl 4-(3-bromopropyl)piperidine-1-carboxylate → HCID 20740364, compound

https://huagongshe.com/reaction/1883165

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(3-bromopropyl)piperidine-1-carboxylateHCID 18409081—
ReactantHCID 131724476HCID 131724476—
ProductHCID 20740364HCID 20740364—

Reaction Steps

Proceeding as described in Example 54, Step 3, 673 mg of 4-(3-bromo-propyl)-piperidine-1-carboxylic acid tert-butyl ester (2.2 mmol) was conyerted to approximately 180 mg 1-(3-Piperidin-4-yl-propyl)-1H-indole-2-carboxylic acid [2-(1-cyano-3-methyl-butylcarbamoyl)-cyclohexyl]-amide, hydrochloride salt (MS: M+H=506; mp=146.4-146.9 C).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759428B2
Source datasetuspto-grants-2004_07
ORD IDord-27571227d6af4214972f2a9cc8bbba58
Source noteuspto-grants-2004_07