HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629916Generated: October 30, 2026
Diisobutylaluminum hydride → HCID 71136786, compound
https://huagongshe.com/reaction/629916
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | HCID 71117301 | HCID 71117301 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71136786 | HCID 71136786 | — |
Reaction Steps
Ethyl 2-[1-(2,2-dimethylpropyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-5-yl]-3-methylcyclopropanecarboxylate (33-2, 192 mg, 0.55 mmol, 1.0 equiv) was added to anhydrous THF (2.7 mL) and cooled to 0° C. DIBAL-H (2.78 mL, 2.78 mmol, 5.0 equiv, 1.0M in THF) was added dropwise and the resulting solution was stirred at 0° C. for 2 h. The reaction was then quenched by the addition of saturated Rochelle salts (20 mL), diluted with EtOAc (10 mL) and stirred at RT for 18 h. Following this duration, the layers were separated and the aqueous layer was extracted with ethyl acetate (3×10 mL). The combined organics were dried over Na2SO4, filtered and concentrated in vacuo to give a clear, yellow oil. Purification by reverse-phase HPLC (10-100% 0.1% TFA in H2O:CH3CN) provided 35-1 as a colorless oil. MS m/z (M+H): observed=304.1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315518B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-96979f41898e452cb1ddcb293999ec63 |
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| Source note | uspto-grants-2016_04 |
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