HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244866Generated: October 26, 2026
2-{2-[2-ethyl-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]ethenyl}-1H-isoindole-1,3(2H)-dione → 2-{2-[2-ethyl-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]ethyl}-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/reaction/244866
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-{2-[2-ethyl-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]ethenyl}-1H-isoindole-1,3(2H)-dione | HCID 69079583 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-{2-[2-ethyl-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]ethyl}-1H-isoindole-1,3(2H)-dione | HCID 69083119 | 99.9% |
Reaction Steps
A glass Parr vessel was charged with 10% palladium on carbon (0.4 g), methanol (75 mL) and 2-{2-[2-ethyl-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]ethenyl}-1H-isoindole-1,3(2H)-dione (1.9 g, 4.3 mmol). The vessel was evacuated and charged with hydrogen gas (40 psi, 2.8×105 Pa). The reaction was shaken at 50° C. for approximately 18 hours and then cooled to ambient temperature. The reaction mixture was filtered followed by concentration under reduced pressure to provide 1.9 g of 2-{2-[2-ethyl-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]ethyl}-1H-isoindole-1,3(2H)-dione as a bright yellow solid. MS (APCI) m/z 443 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658666B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-ea729c8e380a40c387e995ba28b71452 |
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| Source note | uspto-grants-2014_02 |
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