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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916499Generated: October 31, 2026

1,2-Dichloroethane → HCID 86701074, compound

https://huagongshe.com/reaction/1916499

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 numberUS08618128B1
Source datasetuspto-grants-2013_12
ORD IDord-42b99474c54a40df9ec2f9a6eaf14f2f
Source noteuspto-grants-2013_12