HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179819Generated: October 31, 2026
2,2-Dimethylsuccinic anhydride → HCID 66858177, compound
https://huagongshe.com/reaction/2179819
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2-Dimethylsuccinic anhydride | HCID 87067 | — |
| Reactant | 2-Amino-3,4-dimethylpyridine | HCID 11007884 | — |
| Reactant | HCID 50924701 | HCID 50924701 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66858177 | HCID 66858177 | — |
Reaction Steps
To a stirred solution of tert-butyl 2-(6-(2-((1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysene-3a-carboxamido)ethyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate (Example 79, 0.5 g, 0.80 mmol) in pyridine (5 ml), dimethyl amino pyridine (0.2 g, 1.6 mmol) and 3,3-dimethyldihydrofuran-2,5-dione (0.82 ml) were added. Contents were refluxed for about 16 hours. After completion of the reaction, the reaction mixture was diluted with ethyl acetate (30 ml). The organic layer was washed with 5% aqueous HCl, water followed by brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography using 5% MeOH in DCM as eluent to furnish the title compound (0.25 g) as a white solid. 1H NMR (300 MHz, CDCl3): 0.95-1.16 (m, 19H); 1.23-1.78 (m, 23H); 2.15-2.59 (m, 11H); 2.77-3.58 (m, 16H); 4.33-4.70 (m, 4H); 5.58-5.60 (s, 1H); 5.78-5.80 (s, 1H); 7.44-7.47 (s, 1H); ES Mass: 806 [M+Na].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067966B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-913c75439d854bc98a493dac8c63f3e9 |
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| Source note | uspto-grants-2015_06 |
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