HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877970Generated: October 30, 2026
HCID 66886373, compound → HCID 58827076, compound
https://huagongshe.com/reaction/1877970
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66886373 | HCID 66886373 | — |
| Reactant | HCID 67030329 | HCID 67030329 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58827076 | HCID 58827076 | — |
Reaction Steps
To a solution of 6-(5-allyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine-5-yl)biphenyl-3-carbonitrile (35 mg, 0.103 mmol) in EtOH (2 mL) at ambient temperature is added H2NNH2/THF (1.0 M, 15 mL, 15 mmol) and saturated aqueous CuSO4 (0.1 mL). The reaction mixture is stirred at ambient temperature overnight. The mixture is concentrated and dissolved in EtOAc, which is washed with water, dried over anhydrous Na2SO4 and concentrated to give the crude oil, which is subjected to flash chromatography (silica gel) eluting with MeOH:CH2Cl2 to yield the desired compound. MS (ESI) m/z 342 (M+H); 1H NMR (400 MHz, CDCl3) δ ppm (HCl salt) 0.95 (t, J=7.2 Hz, 3 H), 1.21-1.33 (m, 2 H), 1.80-1.90 (m, 2 H), 1.90-2.02 (m, 1 H), 2.09-2.37 (m, 3 H), 2.59-2.68 (m, 1 H), 2.71-2.85 (m, 1 H), 6.81-6.88 (m, 1 H), 6.90-6.98 (m, 2 H), 7.19-7.25 (m, 1 H), 7.27-7.39 (m, 3 H), 7.43 (d, J=1.8 Hz, 1 H), 7.71 (dd, J=8.3, 2.0 Hz, 1 H), 8.10-8.18 (m, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314097B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-eda7b98b8eed4ee5a27b0db044fc2357 |
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| Source note | uspto-grants-2012_11 |
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