HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-one → HCID 12150153, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-one | HCID 70556 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2-(1,3-Thiazol-2-yl)benzaldehyde | HCID 15532482 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 12150153 | HCID 12150153 | — |
Reaction Steps
To a mixture of 2-(2-thiazolyl)benzaldehyde (200 mg, 1.06 mmol) and 1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one (0.232 mg, 1.00 mmol) in 1,2-dichloroethane (20 mL) was added sodium triacetoxyborohydride (376 mg, 1.79 mmol). The resultant mixture was stirred at room temperature for 18 h, quenched with aqueous NaHCO3 (50 mL) and extracted with CHCl3 (2×50 mL). The organic solution was dried over Na2SO4, filtered and concentrated. The crude product was dissolved in 1:1 CHCl3:CH3OH (30 mL) and treated with 2 mL of 1 N HCl in Et2O. The HCl salt was precipitated by addition of Et2O, collected by filtration and dried in the vacuum oven at 60° C. for 18 h to yield the product as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06777421B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-918881051a294baca162216706de8288 |
| Source note | uspto-grants-2004_08 |