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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562973Generated: October 30, 2026

HCID 57810258, compound → HCID 57810092, compound

https://huagongshe.com/reaction/562973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57810258HCID 57810258—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 57810092HCID 5781009265%

Reaction Steps

(6,7-Dimethoxy-quinazolin-4-yl)-(2-fluoro-4-nitro-phenyl)-amine (673 mg, 1.95 mmol) was dissolved in a combination of DMF (20 ml) and MeOH (20 ml), to which was added 10% Pd/C (227 mg). The mixture was shaken under an atmosphere of H2 on a Parr hydrogenator at 40 psi for 3 hrs. The reaction mixture was filtered through celite and the filtrate concentrated in vacuo. The resulting residue was triturated in EtOAc/Et2O. The resulting solids were filtered, washed with Et2O, and dried under vacuum to give N1-(6,7-dimethoxy-quinazolin-4-yl)-2-fluoro-benzene-1,4-diamine (398 mg, 65%) which was used in the next reaction without further purification. 1H-NMR (400 MHz, DMSO): 10.80 (br s, 1H), 10.30 (br s, 1H), 8.63 (s, 1H), 8.15 (s, 1H), 7.33 (s, 1H), 7.15 (m, 1H), 6.45 (m, 1H), 3.96 (s, 6H). LC/MS Calcd for [M+H]+ 315.1, found 315.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067436B2
Source datasetuspto-grants-2011_11
ORD IDord-80524e0b105d430a9ced7203d42573aa
Source noteuspto-grants-2011_11