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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449439Generated: October 29, 2026

3-[(Methoxycarbonyl)amino]butanoic acid → methyl {3-[7-[2-amino-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl]-3,4-dihydroisoquinolin-2(1H)-yl]-1-methyl-3-oxopropyl}carbamate

https://huagongshe.com/reaction/449439

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[(Methoxycarbonyl)amino]butanoic acidHCID 22406395—
Reactant4-(4-methylpiperazin-1-yl)-6-(1,2,3,4-tetrahydroisoquinolin-7-yl)pyrimidin-2-amine HCl saltHCID 67541489—
Productmethyl {3-[7-[2-amino-6-(4-methylpiperazin-1-yl)pyrimidin-4-yl]-3,4-dihydroisoquinolin-2(1H)-yl]-1-methyl-3-oxopropyl}carbamateHCID 49779834—

Reaction Steps

This compound was prepared by using procedures analogous to those described for the synthesis of Example 41 starting from 3-[(methoxycarbonyl)amino]butanoic acid and 4-(4-methylpiperazin-1-yl)-6-(1,2,3,4-tetrahydroisoquinolin-7-yl)pyrimidin-2-amine HCl salt. Analytic LCMS (M+H)+: m/z=468.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481732B2
Source datasetuspto-grants-2013_07
ORD IDord-6d8c6900a12a4e05b7b0ac97abaeb961
Source noteuspto-grants-2013_07