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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078730Generated: October 31, 2026

Tetrabutylammonium Fluoride → HCID 136016240, compound

https://huagongshe.com/reaction/2078730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 57637393HCID 57637393—
SolventTetrahydrofuranHCID 8028—
ProductHCID 136016240HCID 13601624083%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-bromo-2-(1-tert-butoxycarbonyl-1H-thieno[3,2-c]pyrazol-3-yl)-6-(tert-butyl-dimethyl-silanyloxy)-indole-1-carboxylic acid tert-butyl ester [0.32 g, 49 mmol, Intermediate (64)] in tetrahydrofuran at 0° C. was added a 1.0 M TBAF solution in tetrahydrofuran (0.51 mL, 0.51 mmol). The resulting solution was stirred at 0° C. for 30 minutes. The solvent was removed. The residue was chromatographed through silica gel (dichloromethane/ethyl acetate, 95/05 as eluant) to produce 3-bromo-2-(1-tert-butoxycarbonyl-1H-thieno[3,2-c]pyrazol-3-yl)-6-hydroxy-indole-1-carboxylic acid tert-butyl ester [0.22 g, 83%, Intermediate (65)] as an orange foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928231B2
Source datasetuspto-grants-2011_04
ORD IDord-ee52f6af9bdd4d6ab8abdee930a0f30f
Source noteuspto-grants-2011_04