HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180092Generated: November 1, 2026
Trifluoroacetic acid → HCID 11347930, compound
https://huagongshe.com/reaction/1180092
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Cyclohexanecarboxaldehyde | HCID 16275 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 11300082 | HCID 11300082 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11347930 | HCID 11347930 | 40.3% |
Reaction Steps
2-(2-Amino-pyrimidin-4-yl)-1,5,6,7-tetrahydro-pyrrolo[3,2-c]pyridin-4-one (140 mg, 0.61 mmol), trifluoroacetic acid (565 μl, 7.33 mmol), and cyclohexanecarbaldehyde (151 μl, 1.25 mmol) were mixed in DMF (10 ml). Sodium triacetoxyborohydride (390 mg, 1.84 mmol) was added to the above solution and the reaction mixture stirred at room temperature under N2 for 20 h. Additional cyclohexanecarbaldehyde (151 μl, 1.25 mmol) and sodium triacetoxyborohydride (390 mg, 1.84 mmol) were added and the reaction mixture was stirred 20 hours longer. The reaction was quenched with 0.33N NaOH (50 ml), and the product was extracted with DCM (50 ml). The DCM extract was dried (MgSO4), and the solvent was evaporated. The residue was purified by flash chromatography (DCM-MeOH, 95:5) to give the product as a beige solid (80 mg, 40% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07279575B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-2e2a255fac514774842b1c94adcb4c93 |
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| Source note | uspto-grants-2007_10 |
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