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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364066Generated: October 30, 2026

HCID 66958142, compound → Tert-butyl 3-[(3-amino-7-benzyloxy-quinolin-4-yl)amino]propylcarbamate

https://huagongshe.com/reaction/1364066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66958142HCID 66958142—
CatalystPlatinumHCID 23939—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 3-[(3-amino-7-benzyloxy-quinolin-4-yl)amino]propylcarbamateHCID 6695847493.5%

Reaction Steps

tert-Butyl 3-[(7-benzyloxy-3-nitroquinolin-4-yl)amino]propylcarbamate (60.0 g, 132.6 mmol) was dissolved in ethyl acetate (400 mL) and transferred to a Parr hydrogenation vessel charged with 5% platinum on carbon (15.6 g, 80 mmol, 0.03 eq). The vessel was purged with nitrogen gas and placed under hydrogen pressure (50 psi, 3.45×105 Pa) overnight. The catalyst was removed by filtration through a layer of CELITE filter aid, and the filter cake was rinsed with methanol and dichloromethane. The filtrate was concentrated under reduced pressure to provide 52.4 g of tert-butyl 3-[(3-amino-7-benzyloxy-quinolin-4-yl)amino]propylcarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888349B2
Source datasetuspto-grants-2011_02
ORD IDord-d70bb33c4fd54a84a69ae3c93b06bcc6
Source noteuspto-grants-2011_02