HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → ((2S,5R)-1-(4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-6-(4-nitrophenyl)-1,3,5-triazin-2-yl)pyrrolidine-2,5-diyl)dimethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Oxa-8-azabicyclo(3.2.1)octane hydrochloride | HCID 53401129 | — |
| Reactant | HCID 86636521 | HCID 86636521 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ((2S,5R)-1-(4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-6-(4-nitrophenyl)-1,3,5-triazin-2-yl)pyrrolidine-2,5-diyl)dimethanol | HCID 67021926 | — |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
A suspension of ((2S,5R)-1-(4-chloro-6-(4-nitrophenyl)-1,3,5-triazin-2-yl)pyrrolidine-2,5-diyl)dimethanol (0.91 g, 2.5 mmol), 3-oxa-8-azabicyclo[3.2.1]octane hydrochloride (0.37 g, 2.5 mmol) in ethanol (13 mL) was treated with triethylamine (1 mL) and heated in a microwave reactor for 20 minutes at 130° C. The reaction mixture was purified by automated flash chromatography (methanol/chloroform) to provide the title compound as a hard peach colored foam. MS (ES+)=443.2 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08445486B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-39a757afa32b43cdbb0ebd2f2b08a912 |
| Source note | uspto-grants-2013_05 |