HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 2-Amino-6,6-dimethylfuro[3,4-d]thiazol-4(6h)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl 6,6-dimethyl-4-oxo-4,6-dihydrofuro[3,4-d]thiazol-2-ylcarbamate | HCID 86618914 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Amino-6,6-dimethylfuro[3,4-d]thiazol-4(6h)-one | HCID 87518986 | 100.2% |
Reaction Steps
To a solution of Example 5A (7.4 g, 26.0 mmol) in dichloromethane (20 mL) was added trifluoroacetic acid (20.0 ml, 260 mmol) slowly at 0° C. The reaction mixture was removed from the ice bath, allowed to reach room temperature and stirred for 3 hours. The reaction mixture was concentrated to dryness, diluted with ethyl acetate (100 mL) and neutralized with saturated NaHCO3 solution. The layers were separated and the aqueous layer was extracted with ethyl acetate (5×100 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated to give 4.8 g (99%) of product as a white solid. MS (ESI+) m/z 185 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735434B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-8bc88f3676a84eb8a20a60aff0dff2e9 |
| Source note | uspto-grants-2014_05 |