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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161805Generated: October 29, 2026

Ethyl Acetate → Methyl 6-amino-4-(4-bromo-2-chlorophenylamino)-5-chloronicotinate

https://huagongshe.com/reaction/1161805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantMethyl 6-azido-4-(4-bromo-2-chlorophenylamino)-5-chloronicotinateHCID 59519382—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductMethyl 6-amino-4-(4-bromo-2-chlorophenylamino)-5-chloronicotinateHCID 59519500—

Reaction Steps

To a suspension of methyl 6-azido-4-(4-bromo-2-chlorophenylamino)-5-chloronicotinate (316 mg, 0.76 mmol) in a mixture of DCM (6 ml) and AcOH (2 ml) was added Zn dust (255 mg, 3.9 mmol) in small portions. After complete addition it was furthers stirred at room temperature for 30 min. Then, the mixture was poured into EtOAc (30 ml), washed with H2O, saturated sodium bicarbonate solution and brine. The organic fractions were dried with Na2SO4 and the solvents were removed and the product was dried in oil-pump vacuo (246 mg, 83%). Rf (CHCl3/MeOH 30:1)=0.3. 1H-NMR (500 MHz, DMSO-D6): δ=9.17 (s, 1H), 8.45 (s, 1H), 7.70-7.70 (d, 1H), 7.38-7.36 (dd, 1H), 7.1 (s, 1H, br), 6.68-6.67 (d, 1H), 3.76 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820664B2
Source datasetuspto-grants-2010_10
ORD IDord-608bf31e25c9489d9e7140a3804b097a
Source noteuspto-grants-2010_10