HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Phenylenediamine → 6-(1H-benzo[d]imidazol-2-yl)pyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Aminopyridine-4-carboxylic acid | HCID 278396 | — |
| Reactant | 6-Aminopyridine-2-carboxylic acid | HCID 351652 | — |
| Reactant | 5-Aminonicotinic Acid | HCID 354316 | — |
| Product | 6-(1H-benzo[d]imidazol-2-yl)pyridin-2-amine | HCID 59679865 | 61.6% |
Reaction Steps
A suspension of 6-aminopyridine-2-carboxylic acid (112 mg), or 2-aminopyridine-4-carboxylic acid (112 mg, 0.82 mmol), or 5-aminopyridine-3-carboxylic acid (112 mg, 0.82 mmol) with 1,2-diaminobenzene (177 mg, 1.64 mmol) was heated in 4 mL of PPA (180 degree) for 2 h. The reaction mixture was each poured into 50 mL ice-water and neutralized with 2 N NaOH (chilled) during vigorous stirring. The resulting precipitate was filtered and washed with 20 mL warm water to afford 105 mg of desired 6-(1H-benzo[d]imidazol-2-yl)pyridin-2-amine (MS, M++H=211.1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088928B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-1af375157da243288daf219d966cdbe2 |
| Source note | uspto-grants-2012_01 |