Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986335Generated: October 31, 2026

tert-Butyl 4-(3-aminopropyl)piperidine-1-carboxylate → 2-[5-Methyl-2-(3-piperidin-4-yl-propylamino)-pyrimidin-4-yl]-benzo[b]thiophene-6-carboxylic acid dimethylamide di-hydrochloride

https://huagongshe.com/reaction/1986335

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(3-aminopropyl)piperidine-1-carboxylateHCID 22990164—
Reactant2-[5-Methyl-2-(2-piperidin-4-ylethylamino)-pyrimidin-4-yl]-benzo[b]thiophene-6-carboxylic acid methylamide di-hydrochlorideHCID 68857425—
Reactant2-(2-Chloro-5-methylpyrimidin-4-yl)-benzo[b]thiophene-6-carboxylic acid dimethylamideHCID 86625362—
Product2-[5-Methyl-2-(3-piperidin-4-yl-propylamino)-pyrimidin-4-yl]-benzo[b]thiophene-6-carboxylic acid dimethylamide di-hydrochlorideHCID 68857098—

Reaction Steps

Using the method of 2-[5-methyl-2-(2-piperidin-4-ylethylamino)-pyrimidin-4-yl]-benzo[b]thiophene-6-carboxylic acid methylamide di-hydrochloride, the title compound is synthesized from 2-(2-chloro-5-methylpyrimidin-4-yl)-benzo[b]thiophene-6-carboxylic acid dimethylamide and 4-(3-aminopropyl)-piperidine-1-carboxylic acid tert-butyl ester and isolated as a foam. ES+(m/z) 438 [M(free base)+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547691B2
Source datasetuspto-grants-2009_06
ORD IDord-bd51d8ccc8064304a43a134b6c83ee67
Source noteuspto-grants-2009_06