HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173433Generated: October 30, 2026
2,5-Diazabicyclo[4.1.0]heptane-2-carboxylic Acid DiMethylethyl Ester → HCID 131732970, compound
https://huagongshe.com/reaction/2173433
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,5-Diazabicyclo[4.1.0]heptane-2-carboxylic Acid DiMethylethyl Ester | HCID 50986452 | — |
| Reactant | 4-Methyl-5-((2R)-oxiran-2-yl)-2-benzofuran-1(3H)-one | HCID 59568646 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131732970 | HCID 131732970 | — |
Reaction Steps
In a microwave vial charged with stirring bar, tert-butyl (±)-2,5-diazabicyclo[4.1.0]heptane-2-carboxylate (341 mg, 1.72 mmol) was dissolved in EtOH (20 mL). 4-methyl-5-[(2R)-oxiran-2-yl]-2-benzofuran-1(3H)-one (654 mg, 3.44 mmol) was added. Then mixture was sealed and put on microwave reactor. It was heated up to 145° C. and was stir at 145° C. for 60 minutes. After cooling down to room temperature, solution was transferred to a round bottom flask and was concentrated on rotavapor to give crude product, which was purified by ISCO (80 gram silica gel column, eluted by 0-10% MeOH/DCM gradient). Removing solvent gave the title compound. LC/MS: (M+1)+=389.14;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056859B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-701b714595b740d99dfcb4e872fadfa2 |
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| Source note | uspto-grants-2015_06 |
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