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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040947Generated: October 30, 2026

N-Methylethylenediamine → HCID 67264659, compound

https://huagongshe.com/reaction/1040947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylethylenediamineHCID 8014—
ReactantSodium CarbonateHCID 10340—
ReactantMethyl 2-chloro-3-nitrobenzoateHCID 10751184—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
ProductHCID 67264659HCID 6726465924%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Chloro-3-nitro-benzoic acid methyl ester (500 mg, 2.32 mmol) was dissolved in n-butanol (2.5 ml). Na2CO3 (246 mg, 2.32 mmol) was added followed by N, methylethylenediamine (204 μL, 2.32 mmol). The reaction mixture was heated to 80° C. for 16 h. The reaction mixture was cooled and diluted with water (50 ml). The resulting mixture was extracted with EtOAc (3×50 mL), dried over MgSO4, and concentrated. Silica gel chromatography (0-100% EtOAc in hexanes) afforded 1-Methyl-9-nitro-1,2,3,4-tetrahydro-benzo[e][1,4]diazepin-5-one as a bright orange solid (114 mg, 24%). Cmp 183-184° C.; LCMS: m/z=222.25 (M+H+) 1H NMR (400 MHz, CDCl3) δ 8.68 (bs, 1H), 8.32 (dd, J=8.4 Hz, 1.8 Hz, 1H), 8.15 (dd, J=7.8 Hz, 1.5 Hz, 1H), 6.78 (t, J=8.3 Hz, 1H), 3.79 (m, 2H), 3.63 (m, 2H), 3.20 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552186B2
Source datasetuspto-grants-2013_10
ORD IDord-301dd4e4e15d4b5a8983789595dfb057
Source noteuspto-grants-2013_10