HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848533Generated: October 31, 2026
Diisopropylethylamine → HCID 86709525, compound
https://huagongshe.com/reaction/1848533
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Methyl-5-((2R)-oxiran-2-yl)-2-benzofuran-1(3H)-one | HCID 59568646 | — |
| Reactant | 3-Methyl-2-(5-oxo-2,5-dihydrofuran-3-yl)-2,8-diazaspiro[4.5]decan-1-one | HCID 86709458 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86709525 | HCID 86709525 | — |
Reaction Steps
3-Methyl-2-(5-oxo-2,5-dihydrofuran-3-yl)-2,8-diazaspiro[4.5]decan-1-one (I-22, 0.257 mmol) was dissolved in ethanol (3 mL), and treated with diisopropylethylamine (135 μl, 0.771 mmol) followed by (R)-4-methyl-5-(oxiran-2-yl)isobenzofuran-1(3H)-one (I-4B, 73.3 mg, 0.385 mmol). The mixture was heated at 80° C. in a sealed tube for 12 hours. The reaction mixture was then cooled to room temperature and concentrated. The resulting crude product was purified by column chromatography eluting with a 0-20% MeOH/EtOAc gradient to give the title product as a mixture of diastereomers. LC-MS (IE, m/z): 441.3 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952166B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-495d64835a354bc193fc7e31b2179159 |
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| Source note | uspto-grants-2015_02 |
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