HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-methyl-5-(oxiran-2-yl)isobenzofuran-1(3H)-one → HCID 49800470, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-methyl-5-(oxiran-2-yl)isobenzofuran-1(3H)-one | HCID 55270555 | — |
| Reactant | HCID 59568694 | HCID 59568694 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 49800470 | HCID 49800470 | — |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
A mixture of isomer (37B) of 5-[2-(3,8-diazabicyclo[3.2.1]oct-3-yl)-1-hydroxyethyl]-4-methyl-2-benzofuran-1(3H)-one (45 mg, 0.149 mmol) and 4-methyl-5-oxiran-2-yl-2-benzofuran-1(3H)-one (57 mg, 0.210 mmol) in 2 mL DMSO was heated under microwave condition (150° C.) for 1 hr. After cooling to rt., the mixture was diluted with water (50 mL), and extracted with EtOAc (3×50 mL). The combined organic layers were washed with brine and dried over Na2SO4, then concentrated. The residue was purified by prep-TLC (MeOH/DCM=1:15) and then separated by SFC chiral chromatography to obtain two separated isomers C and D of 5,5′-[3,8-diazabicyclo[3.2.1]octane-3,8-diylbis(1-hydroxyethane-2,1-diyl)]bis(4-methyl-2-benzofuran-1(3H)-one).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09018211B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-edd19cc964a34befbe029ed8a7c03304 |
| Source note | uspto-grants-2015_04 |