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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808513Generated: November 2, 2026

5-(7-methoxy-6-(3-morpholinopropoxy)-2-(3-nitrophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate → HCID 59361879, compound

https://huagongshe.com/reaction/1808513

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(7-methoxy-6-(3-morpholinopropoxy)-2-(3-nitrophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylateHCID 66826459—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 59361879HCID 59361879—

Reaction Steps

To a mixture of 5-(7-methoxy-6-(3-morpholinopropoxy)-2-(3-nitrophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate (0.215 g) in MeOH (60 mL) was added Pd/C (0.21 g) and NH4CO2 (0.21 g). The mixture was heated at 60° C. for 40 mins, upon which an additional portion of NH4CO2 (0.095 g) was added, heating was continued for a further 20 minutes. The mixture was filtered to remove the Pd/C and the filtrate was concentrated under reduced pressure. The residue was taken up in CH2Cl2 (300 mL) wand was washed with water and brine. The mixture was dried (Na2SO4) and the volatiles removed in vacuo. The material was combined with an identical experiment using 0.2 g and the residue was subjected to preparative TLC (SiO2, CH2Cl2:MeOH 9:1) to give the desired product tert-butyl 5-(2-(3-aminophenyl)-7-methoxy-6-(3-morpholinopropoxy)quinazolin-4-ylamino)-1H-indazole-1-carboxylate. HPLC retention time 4.67 mins.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357693B2
Source datasetuspto-grants-2013_01
ORD IDord-9a16ea372ce749178ec48eecbbb101d9
Source noteuspto-grants-2013_01