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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416270Generated: October 27, 2026

1,2-Dichloroethane → N,1-dimethyl-5-nitro-1H-1,3-benzodiazol-2-amine

https://huagongshe.com/reaction/416270

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantMethyl isothiocyanateHCID 11167—
Reactant1-N-methyl-4-nitrobenzene-1,2-diamineHCID 3420025—
SolventPyridineHCID 1049—
ProductN,1-dimethyl-5-nitro-1H-1,3-benzodiazol-2-amineHCID 5339649462.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of diamine 248 (1.88 g, 11.2 mmol) in pyridine (20 mL) was treated with methyl isothiocyanate (970 mg, 12.9 mmol) and the mixture was stirred at 80° C. for 30 minutes, cooled down to 15° C., treated with solid EDC (3.03 g, 15.8 mmol, 1.40 eq) and the heating continued at 80° C. for 16 h. After removal of pyridine in vacuo, the residue was purified by flash chromatography (eluent 5% MeOH in CH2Cl2) to afford the title compound 268 (1.44 g, 62% yield). 1H NMR: (CD3OD) δ (ppm): 8.12 (d, J=2.2 Hz, 1H), 7.94 (dd, J=2.2, 8.8 Hz, 1H), 7.04 (d, J=8.8 Hz, 1H), 4.44 (bs, 2H), 3.51 (s, 3H), 3.04 (s, 3H). LRMS: (calc.) 206.2; (obt.) 207.1 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088805B2
Source datasetuspto-grants-2012_01
ORD IDord-a8f1d722bdd64dc48984258410fa855c
Source noteuspto-grants-2012_01