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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383155Generated: October 30, 2026

Isopropanol → Tert-butyl [4-(3-amino-7-benzyloxyquinolin-4-ylamino)butyl]carbamate

https://huagongshe.com/reaction/2383155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantHCID 69027554HCID 69027554—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventTolueneHCID 1140—
ProductTert-butyl [4-(3-amino-7-benzyloxyquinolin-4-ylamino)butyl]carbamateHCID 68900070108.8%

Reaction Steps

tert-Butyl[4-(7-benzyloxy-3-nitroquinolin-4-ylamino)butyl]carbamate (20.36 g, 43.6 mmol) was slurried in toluene (450 mL) and added to a Parr vessel charged with 5% platinum on carbon (4.3 g) and a small amount of toluene. 2-Propanol (50 mL) was added, and the vessel was charged with hydrogen (30 psi, 2.1×105 Pa). The hydrogen was replaced three times. After 4 hours, the catalyst was removed by filtration through a layer of CELITE filter aid, and the filter cake was rinsed with toluene (0.5 L), 50% toluene/2-propanol (0.5 L), and 2-propanol (0.25 L). The filtrate was concentrated under reduced pressure, and the residue was mixed with toluene and concentrated under reduced pressure to provide 20.7 g of tert-butyl[4-(3-amino-7-benzyloxyquinolin-4-ylamino)butyl]carbamate as a viscous, black oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263594B2
Source datasetuspto-grants-2012_09
ORD IDord-2b3e91a1fdf3469bb1b094e4bc978ba3
Source noteuspto-grants-2012_09