HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 16048691, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 66930842 | HCID 66930842 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 16048691 | HCID 16048691 | — |
Reaction Steps
A solution of 3-[4-(5,6,7,8-tetrahydropyrazolo[3,4-d]azepin-2(4H)-yl)phenyl]-1,3-oxazolidin-2-one (25.0 mg, 0.08 mmol) (may be prepared as described in Description 27) in dichloromethane (3 ml) was treated with acetone (25.0 μl, 0.34 mmol) and acetic acid (1 drop) and stirred at room temperature. Sodium triacetoxyborohydride (72.0 mg, 0.34 mmol) was added and the mixture stirred for 3 hours and then overnight. The mixture was diluted with methanol and passed down a SCX cartridge eluting with methanol and then a 2M solution of ammonia in methanol. The basic fractions were combined and evaporated to afford the title compound (E9); MS (ES+) m/e 341 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07888347B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-9b658a6298134e9d9708f67495c4cae8 |
| Source note | uspto-grants-2011_02 |