HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852949Generated: October 27, 2026
1,2-Dichloroethane → N,1-dimethyl-5-nitro-1H-1,3-benzodiazol-2-amine
https://huagongshe.com/reaction/852949
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Methyl isothiocyanate | HCID 11167 | — |
| Reactant | 1-N-methyl-4-nitrobenzene-1,2-diamine | HCID 3420025 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N,1-dimethyl-5-nitro-1H-1,3-benzodiazol-2-amine | HCID 53396494 | 62.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253204B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-3faec59ff25b48aa8f42812e6082df4e |
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| Source note | uspto-grants-2007_08 |
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