HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → N-(benzo[d]thiazole-2-yl)-2-(2H-tetrazole-5-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | N-(1,3-benzothiazol-2-yl)-2-cyanoacetamide | HCID 4530340 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(benzo[d]thiazole-2-yl)-2-(2H-tetrazole-5-yl)acetamide | HCID 86660694 | 20% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
N-(benzo[d]thiazole-2-yl)-2-cyanoacetamide (0.1 g), NH4Cl (5.0 eq, 0.1 g), and NaN3 (5.2 eq, 0.13 g) were dissolved on 2.1 mL of DMF (dimethylformamide), and heated at 120° C. for 6 hours. DMF was removed under reduced pressure distillation, and 10 ml of water and 5% NaOH solution were added thereto. The aqueous layer was washed with 15 ml of Et2O, and treated with activated carbon. To the obtained reaction mixture, 10% aqueous hydrochloric acid, making the solution with pH 2. The obtained reaction mixture was extracted with methylene chloride, to produce N-(benzo[d]thiazole-2-yl)-2-(2H-tetrazole-5-yl)acetamide (20%, 21 mg) in light yellow solid phase.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09012481B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-5ebc77ace50a49899e646e4287a3be39 |
| Source note | uspto-grants-2015_04 |