HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591348Generated: October 30, 2026
Diisobutylaluminum hydride → HCID 71657340, compound
https://huagongshe.com/reaction/591348
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | HCID 45051801 | HCID 45051801 | — |
| Reactant | HCID 89612672 | HCID 89612672 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71657340 | HCID 71657340 | — |
Reaction Steps
To a suspension of ethyl 2-(4-(6-fluoroindolin-1-yl)piperidine-1-carboxamido)thiazole-4-carboxylate (83.6 mg, 0.2 mmol, 1 equiv) in dried CH2Cl2 (3 mL) under N2 at room temperature was then slowly added DIBAL-H (1M in CH2Cl2, 1 mL, 1 mmol, 5 equiv). The resulting mixture became a clear solution and was stirred at room temperature for 1 h. The resulting mixture was slowly poured into a vigorously stirred mixture of CH2Cl2/10 wt % sodium tartaric acid (aq.) (10 mL/10 mL). The resulting mixture was stirred for 1 h and the layers were separated. The aqueous layer was extracted with CH2Cl2 (30 mL). The combined organic layer was dried (Na2SO4) and filtered. The solvent was removed by roto-evaporator and the resulting residue purified by column using 80-90% EtOAc/hexane as the eluent to yield 4-(6-fluoroindolin-1-yl)-N-(4-(hydroxymethyl)thiazol-2-yl)piperidine-1-carboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238658B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-5de3c7fc9cac4c53b7e44b6b61db1cb6 |
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| Source note | uspto-grants-2016_01 |
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