Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189659Generated: October 30, 2026

HCID 57470253, compound → tert-Butyl 7-amino-4,4-dimethyl-3,4-dihydroquinoline-1(2H)-carboxylate

https://huagongshe.com/reaction/2189659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57470253HCID 57470253—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl 7-amino-4,4-dimethyl-3,4-dihydroquinoline-1(2H)-carboxylateHCID 5735499695%

Reaction Steps

A mixture of 4,4-dimethyl-7-nitro-3,4-dihydro-2H-quinoline-1 carboxylic acid tert-butyl ester (8.3 g, 0.03 mol) and Pd—C (0.5 g) in methanol (100 mL) was stirred under H2 (1 atm) at room temperature overnight. The catalyst was filtered off and the filtrate was concentrated. The residue was washed with petroleum ether to give tert-butyl 7-amino-3,4-dihydro-4,4-dimethylquinoline-1(2H)-carboxylate (DC-3) (7.2 g, 95%). 1H NMR (CDCl3) δ 7.11-7.04 (m, 2H), 6.45-6.38 (m, 1H), 3.71-3.67 (m, 2H), 3.50-3.28 (m, 2H), 1.71-1.67 (m, 2H), 1.51 (s, 9H), 1.24 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324242B2
Source datasetuspto-grants-2012_12
ORD IDord-eb51f35de490487a9acb7f89d8ff0c82
Source noteuspto-grants-2012_12