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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472194Generated: November 2, 2026

1,2-Dichloroethane → HCID 86701074, compound

https://huagongshe.com/reaction/1472194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantEthylamine hydrochlorideHCID 11198—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-3-nitrobenzoic acidHCID 219633—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 86701074HCID 8670107447.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-amino-3-nitrobenzoic acid (CXXVI) (366 mg, 2.0 mmol) in DCM (5 mL) and DMF (1 mL) was added ethylamine hydrochloride and EDC. The mixture was cooled to 0° C. under argon before added DIPEA. The reaction was stirred at room temperature for 3 h. The solution was concentrated under vacuum, dissolved in water and extracted with EtOAc. The combined organic phases were washed with brine, dried over MgSO4 and concentrated under vacuum. The residue was purified on a silica gel column (100% CHCl3→5:95 MeOH[7N NH3]:CHCl3) to give 4-amino-N-ethyl-5-nitronicotinamide (CXXVII) as a yellow solid (200 mg, 0.95 mmol, 47.6% yield). 1H NMR (DMSO-d6, 500 MHz) δ ppm 1.14 (t, J=7 Hz, 3H), 3.28 (q, J=6 Hz, 2H), 8.97 (s, 1H), 9.06 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012472B2
Source datasetuspto-grants-2015_04
ORD IDord-2e2bc5f3397c4f27a0986923dc7cf61b
Source noteuspto-grants-2015_04