HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → (1S,6R)-3,8-diazabicyclo[4.2.0]octan-8-yl(3-fluoro-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | (1S,6R)-tert-butyl 8-(3-fluoro-2-(2H-1,2,3-triazol-2-yl)benzoyl)-3,8-diazabicyclo[4.2.0]octane-3-carboxylate | HCID 67086535 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1S,6R)-3,8-diazabicyclo[4.2.0]octan-8-yl(3-fluoro-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone | HCID 67086539 | — |
Reaction Steps
To (1S,6R)-tert-butyl 8-(3-fluoro-2-(2H-1,2,3-triazol-2-yl)benzoyl)-3,8-diazabicyclo[4.2.0]octane-3-carboxylate (656 mg, 1.6 mmol) in CH2Cl2 (10 mL) was added TFA (10 mL). After 3 h, the volatiles were removed via rotovap. The resulting residue was neutralized using 5% Na2CO3 (aq) and extracted with CH2Cl2 (3×). The aqueous layer was saturated with NaCl and extracted with CH2Cl2 (3×). The combined organics were dried (Na2SO4) and concentrated to give the title compound as a yellow foam that was used without further purification. MS (ESI) mass calcd. C15H16FN5O, 301.32; m/z found 302.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062044B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-ecc6534998764bffa200f0c056eb74f3 |
| Source note | uspto-grants-2015_06 |