HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-1,2-diaminobenzene → N-(2-amino-4-chlorophenyl)-6-chloronicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-1,2-diaminobenzene | HCID 7263 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Chloronicotinic acid | HCID 79222 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | N-(2-amino-4-chlorophenyl)-6-chloronicotinamide | HCID 22668939 | 48% |
Reaction Steps
6-Chloronicotinic acid (157.5 mg, 1 mmol) and 8 ml of DMF were stirred at room temperature while 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (384 mg, 2 mmol), hydroxybenzotriazole (162 mg, 1.2 mmol), triethylamine (404 mg, 4 mmol) and 4-chloro-o-phenylenediamine (171 mg, 1.2 mmol) were added. The mixture was stirred for 20 hours at room temperature. The mixture was diluted with 400 mL of brine and extracted with 200 ml of ethyl acetate. The ethyl acetate was removed under vacuum. To the residue was added 5 ml of absolute ethanol. The solids were collected by vacuum filtration, washed with absolute ethanol and dried under vacuum to give the title compound (135 mg, 48% yield) as a brown solid. LC-MS (m/z) 282 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158656B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-962de30396b64265b5287ca0bd306bc4 |
| Source note | uspto-grants-2012_04 |