HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzothiazole → HCID 22767696, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzothiazole | HCID 11987 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178508668 | HCID 178508668 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22767696 | HCID 22767696 | — |
Reaction Steps
To 3.98 g. 7H-pyrrolo[3,2-f]quinazoline-1,3-diamine dissolved in 250 ml. dry dimethylformamide are added, with stirring under nitrogen, 1.15 g. ca. 50% sodium hydride-mineral oil dispersion. After stirring for 1.5 hours, 3.90 g. 2-chlorobenzothiazole are added and the mixture is heated at 95° for 3 hours. An additional 1.29 g. 2-chlorobenzothiazole are added and heating at 95° is continued for 11 hours. A third portion of 2-chlorobenzothiazole (1.29 g.) is added and heating at 95° is continued for 8 hours. The reaction mixture is processed as in Example 69 and the crude product is recrystallized (twice) from dimethylformamide and is thoroughly dried to yield 2.30 g. title compound, m.p. 326° (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04118561 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-4cf74bbc1272433091555757c33fd7c3 |
| Source note | uspto-grants-1978_10 |