HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 52939884, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 52939883 | HCID 52939883 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 52939884 | HCID 52939884 | 46% |
Reaction Steps
To a solution of 5-cyclopropyl-1-(2-(4-fluorophenyl)-2-oxoethyl)-8-methoxy-2,3,5,6-tetrahydrobenzo[b][1,5]diazocin-4(1H)-one (65.0 mg, 0.170 mmol) from Example 5 in ethanol (1 ml) was added sodium borohydride (6.4 mg, 0.170 mmol) and the reaction mixture was stirred at room temperature over weekend. Then was added acetone (0.062 ml) followed by dilution with dichloromethane. The resulting solution was washed with water and the organic phase was dried over sodium sulfate and filtered. Evaporation gave the desired product (30 mg, 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765728B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-e803529905e74d3794b9fc2f21ac6749 |
| Source note | uspto-grants-2014_07 |