Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | 3,4-Dihydro-2H-pyrimido[2,1-b][1,3]benzothiazol-7-amine | HCID 13338584 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13338632 | HCID 13338632 | — |
Reaction Steps
To a stirred solution of 3 parts of 3,4-dihydro-2-H-pyrimido[2,1-b]benzothiazol-7-amine in 16 parts of acetic acid are added 32 parts of water. Then there is added dropwise a solution of 1.46 parts of potassium cyanate in 32 parts of water (slightly exothermic reaction). Upon completion, stirring is continued overnight at room temperature. The reaction mixture is alkalized with ammonium hydroxide and the whole is stirred while cooling at 10° C. The precipitated product is filtered off and crystallized twice: first from 2-methoxyethanol and then from 1-butanol, yielding 0.6 parts of N-(3,4-dihydro-2H-pyrimido[2,1-b]benzothiazol-7-yl)urea; mp. 245.9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04471117 |
|---|
| Source dataset | uspto-grants-1984_09 |
|---|
| ORD ID | ord-a74a2a4bfcb443bd8ebda9c7b9d45d5d |
|---|
| Source note | uspto-grants-1984_09 |
|---|