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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727613Generated: October 30, 2026

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

https://huagongshe.com/reaction/1727613

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-1carboxylic 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, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495103B2
Source datasetuspto-grants-2009_02
ORD IDord-952ab56552d14163b81797c4be7275fa
Source noteuspto-grants-2009_02