HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993491Generated: October 31, 2026
HCID 67245490, compound → HCID 59134307, compound
https://huagongshe.com/reaction/1993491
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67245490 | HCID 67245490 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 59134307 | HCID 59134307 | — |
Reaction Steps
To a solution of (3R*,4S*)-3-hydroxy-2,2,9-trimethyl-4-[(2-phenylethyl)amino]-3,4-dihydro-2H-pyrano[2,3-g]quinoline-7-carbonitrile described in Synthesis Example 14(110 mg, 0.283 mmol) in acetic acid (5 mL), 10% Pd/C (22 mg) was added at room temperature, and the resulting mixture was stirred for 2 hours under hydrogen atmosphere. Upon the completion of the reaction, the resulting solution was filtered through celite, the solvent was distilled off and then aqueous sodium carbonate solution was added to the residue, and the resulting solution was extracted with chloroform, dried over anhydrous magnesium sulfate, and the solvent was distilled off to obtain crude product of (3R*,4S*)-7-aminomethyl-2,2,9-trimethyl-4-[(2-phenylethyl)amino]-3,4-dihydro-2H-pyrano[2,3-g]quinolin-3-ol (75.1 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652008B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-d63d7ee87e534164af07e544ae698035 |
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| Source note | uspto-grants-2010_01 |
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