HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoacetamide → 2-[2-Imino-6-(trifluoromethoxy)-1,3-benzothiazol-3(2H)-yl]ethanimidic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoacetamide | HCID 3727 | — |
| Reactant | Riluzole | HCID 5070 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 2-[2-Imino-6-(trifluoromethoxy)-1,3-benzothiazol-3(2H)-yl]ethanimidic acid | HCID 3076412 | 53% |
Reaction Steps
The procedure is as in Example 15, starting with 2-amino-6-trifluoromethoxybenzothiazole (9.4 g) and iodoacetamide (14.8 g) in methyl ethyl ketone (50 cc). The mixture is heated for 18 hours to boiling and then cooled to a temperature in the region of 20.C. The precipitate formed is filtered off, then added to distilled water (100 cc) and treated with IN sodium hydroxide (37 cc). The insoluble matter is filtered off, washed with distilled water (100 cc) and recrystallized in boiling methanol (100 cc). (2-Imino-6-trifluoromethoxy-3-benzothiazolinyl)acetamide (6.2 g), m.p. 228° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05026717 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-57ce784e5da44225a5279cacdcf53993 |
| Source note | uspto-grants-1991_06 |