HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 2-p-Tolyl-imidazo[2,1-b]benzothiazol-7-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 7-Nitro-2-p-tolyl-imidazo[2,1-b]benzothiazole hydrobromide salt | HCID 68818552 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-p-Tolyl-imidazo[2,1-b]benzothiazol-7-ylamine | HCID 11637706 | 22% |
Reaction Steps
To a suspension of 7-Nitro-2-p-tolyl-imidazo[2,1-b]benzothiazole hydrobromide salt (128 mg, 0.328 mmol) in water at 80° C. were added 4 portions (10 eq.) of sodium dithionite over 30 minutes whereupon the suspension become clear and decolorized to give 7 in 22% yield: mp>210° C. (dec.); 1H-NMR (DMSO-d6) 2.32 (s, 3H), 6.80 (dd, 1H), 7.13 (d, 1H), 7.23 (d, 2H), 7.65 (d, 1H), 7.72 (d, 2H), 8.53 (s, 1H); HR-MS (EI) m/z 279.0821 (M+); Anal. calculated for C16H13N3S. 7/3 HBr: C, 41.05; H, 3.30; N, 8.98; found; C, 41.81; H, 2.86; N, 6.10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601846B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-9f29dacd52a04503a834fd2791a02954 |
| Source note | uspto-grants-2009_10 |