HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 13338630, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3,4-Dihydro-2H-pyrimido[2,1-b][1,3]benzothiazol-7-amine | HCID 13338584 | — |
| Product | HCID 13338630 | HCID 13338630 | — |
Reaction Steps
To a stirred mixture of 45 parts of trifluoroacetic acid and 2 parts of 3,4-dihydro-2H-pyrimido[2,1-b]benzothiazol-7-amine are added portionwise, during a 4 hours-period, 3 parts of sodium borohydride at 30°-40° C. while nitrogen gas is introduced. The reaction mixture is poured onto ice-water and the whole is alkalized with ammonium hydroxide. The product is extracted with methylbenzene. The extract is washed with water, dried, filtered and evaporated. The residue is crystallized from 8 parts of acetonitrile, yielding 0.55 parts of 3,4-dihydro-N-(2,2,2-trifluoroethyl)-2H-pyrimido[2,1-b]benzothiazol-7-amine; mp. 186.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04471117 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-c6b05e3ae7d747aeacc482637d0df0c2 |
| Source note | uspto-grants-1984_09 |