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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628103Generated: November 1, 2026

Tetrabutylammonium Fluoride → HCID 58382014, compound

https://huagongshe.com/reaction/1628103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 58382028HCID 58382028—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58382014HCID 5838201439%

Reaction Steps

To a mixture of 2-(4-(8-bromo-1-methyl-6-(triisopropylsilyl)-6H-imidazo[1,5-a]pyrrolo[2,3-e]pyrazin-3-yl)phenyl)propan-2-ol (0.300 g, 0.554 mmol; Preparation #AD.1) in THF (5 mL) was added TBAF (0.504 mL, 0.554 mmol). The mixture was stirred at about rt for about 1 h and then was partitioned between DCM (50 mL) and water (25 mL). The layers were separated and the aqueous phase was extracted with DCM (3×20 mL). The combined organic phases were washed with brine (100 mL) and then the solid was collected by filtration to give 2-(4-(8-bromo-1-methyl-6H-imidazo[1,5-a]pyrrolo[2,3-e]pyrazin-3-yl)phenyl)propan-2-ol (0.082 g, 39%). LC/MS (Table 2, Method a) Rt=1.87 min.; MS m/z: 387 (M+H)+. Syk IC50=A.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785639B2
Source datasetuspto-grants-2014_07
ORD IDord-bec021ad741b4700b6abf1f427d07c68
Source noteuspto-grants-2014_07