HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239741Generated: October 29, 2026
Trifluoroacetic acid → HCID 178492152, compound
https://huagongshe.com/reaction/2239741
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 178472389 | HCID 178472389 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178492152 | HCID 178492152 | 50% |
Reaction Steps
Ethyl 4-{8-[(2-fluorophenyl)amino]-2-[(4-methoxyphenyl)amino]purin-9-yl}-trans-cyclohexanecarboxylate (0.28 g, 0.55 mmol) was dissolved in 9 mL of THF and cooled to 0° C. (under nitrogen atmosphere). 1.38 mL of 1.0M LiAlH4 in THF was added dropwise. The solution turned a dark orange as the LiAlH4 was added. The reaction mixture was stirred for about 5 h and quenched by the addition of 40 mL of water. The reaction was extracted three times with ethyl acetate. Organics were combined and dried with magnesium sulfate, filtered and the solvent was removed in vacuo. The crude reaction mixture was then purified using reverse-phase preparative HPLC (20-80% acetonitrile/water (0.1% TFA) over 30 min) to obtain 0.126 g of the desired product (50% yield) after neutralization of the TFA salt. ES-MS: 463 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723340B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-de8b987b65b34d8fa10846ab9ae3161a |
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| Source note | uspto-grants-2010_05 |
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