HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845717Generated: November 2, 2026
Trifluoroacetic acid → HCID 57568671, compound
https://huagongshe.com/reaction/1845717
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 68923284 | HCID 68923284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57568671 | HCID 57568671 | 53% |
Reaction Steps
A solution of tert-butyl 2-[4-({2-[4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-1,1-dimethylethyl}amino)-4-oxobutanoyl]hydrazinecarboxylate (792 mg, 1.50 mmol) in dichloromethane (30 mL) was treated with trifluoroacetic acid (3 mL). After stirring for 2 hours, additional trifluoroacetic acid (3 mL) was added to the reaction mixture and stirring was continued for 1 hour. The reaction mixture was concentrated under reduced pressure and the resulting syrup was dissolved in water. The solution was made basic by the addition of concentrated ammonium hydroxide and then was extracted repeatedly with 10% methanol/chloroform. The combined organic portions were dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude white solid was purified by chromatography on silica gel (gradient elution, 25%-75% CMA in chloroform) gave 340 mg of N-{2-[4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-1,1-dimethylethyl}-4-hydrazino-4-oxobutanamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08951528B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-024a38d4f8df407aaf91c71d9d6a9578 |
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| Source note | uspto-grants-2015_02 |
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