HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1,3-Dibenzyl-8-methanesulfonyl-1,4,8-triazaspiro[4,5]decan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1,3-Dibenzyl-1,4,8-triazaspiro[4,5]decan-2-one | HCID 68837942 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,3-Dibenzyl-8-methanesulfonyl-1,4,8-triazaspiro[4,5]decan-2-one | HCID 68837760 | — |
Reaction Steps
Triethylamine (0.15 ml, 1.78 mmol) and subsequently methanesulfonyl chloride (0.14 ml, 1.78 mmol) were added to a solution of 1,3-dibenzyl-1,4,8-triazaspiro-[4,5]decan-2-one (300 mg, 0.89 mmol) in CH2Cl2 (8.1 ml) with stirring using nitrogen as an inert gas at RT. The reaction mixture was stirred overnight. The organic phase was rendered alkaline using aqueous sodium carbonate solution (20 ml) and the aqueous phase was extracted with CH2Cl2 (15 ml). The combined organic phases were dried over Na2SO4. After filtration, removal of the solvent, and column chromatography, the desired product 1,3-dibenzyl-8-methanesulfonyl-1,4,8-triazaspiro[4,5]decan-2-one was obtained in a yield of 287 mg (77% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560468B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-7c42931adaa44c64920a7af1ef5adef0 |
| Source note | uspto-grants-2009_07 |