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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446558Generated: October 27, 2026

tert-butyl N-methyl-N-(3-oxopropyl)carbamate → 1-{2-[{6-[(2-{3-([tert-Butoxycarbonyl)(methyl)amino]propyl}-1,2,3,4-tetrahydroisoquinolin-6-yl)amino]hexanoyl}(methyl)amino]ethyl}piperidin-4-yl biphenyl-2-ylcarbamate

https://huagongshe.com/reaction/446558

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-methyl-N-(3-oxopropyl)carbamateHCID 10442454—
Reactant1-(2-{Methyl[6-(1,2,3,4-tetrahydroisoquinolin-6-ylamino)hexanoyl]amino}ethyl)piperidin-4-yl biphenyl-2-ylcarbamateHCID 66671813—
Product1-{2-[{6-[(2-{3-([tert-Butoxycarbonyl)(methyl)amino]propyl}-1,2,3,4-tetrahydroisoquinolin-6-yl)amino]hexanoyl}(methyl)amino]ethyl}piperidin-4-yl biphenyl-2-ylcarbamateHCID 6667136579.4%

Reaction Steps

The compound (47 mg, 78.6 μmol) obtained in Example 63b and tert-butyl methyl(3-oxopropyl)carbamate (Bioorg. Med. Chem., 12, 19, 2004, 5147-5160) (18 mg, 94.3 μmol) were used to give the title compound (48 mg; yield, 79%) as a colorless oily substance according to the method described in Example 41a.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476253B2
Source datasetuspto-grants-2013_07
ORD IDord-88038a6736044a3f8e5f9e388f50af37
Source noteuspto-grants-2013_07