HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 13338631, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3,4-Dihydro-2H-pyrimido[2,1-b][1,3]benzothiazol-7-amine | HCID 13338584 | — |
| Product | HCID 13338631 | HCID 13338631 | — |
Reaction Steps
To 25 parts of acetic acid anhydride are added portionwise 1.3 parts of 3,4-dihydro-2H-pyrimido[2,1-b]benzothiazol-7-amine (exothermic reaction: temp. rises to 30° C.). Upon completion, stirring is continued for one hour at room temperature. After cooling to 5°-10° C., the precipitated product is filtered off and dissolved in water. The solution is treated with activated charcoal. The latter is filtered off over hyflo and the filtrate is alkalized with a few drops of ammonium hydroxide. Upon stirring, the product is allowed to crystallize. It is filtered off and dried, yielding 0.8 parts of N-(3,4-dihydro-2H-pyrimido[2,1-b]benzothiazol-7-yl)acetamide; mp. 178° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04471117 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-6c79ee46d34c4fef968c8a99cf03eb6d |
| Source note | uspto-grants-1984_09 |