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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943877Generated: November 2, 2026

Tetrabutylammonium Fluoride → HCID 178461061, compound

https://huagongshe.com/reaction/1943877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 178461062HCID 178461062—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178461061HCID 17846106152%

Reaction Steps

Tetra-n-butylammonium fluoride (“TBAF”; 0.12 mL, 0.12 mmol, 1.0M in THF) was added to a solution of N-(3-(3-(tert-butyldimethylsilyloxy)propyl)-1H-pyrazolo[3,4-b]pyridin-5-yl)-2,6-difluoro-3-(propylsulfonamido)benzamide (0.034 g, 0.060 mmol) in THF (4.0 mL), and the reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated, and the crude product was purified by column chromatography, eluting with ethyl acetate, ethyl acetate/MeOH (50:1) to give 2,6-difluoro-N-(3-(3-hydroxypropyl)-1H-pyrazolo[3,4-b]pyridin-5-yl)-3-(propylsulfonamido)benzamide (0.014 g, 52%) as a solid. 1H NMR (400 MHz, CD3OD) δ 8.7 (s, 1H), 8.6 (s, 1H), 7.7 (m, 1H), 7.1 (m, 1H), 3.7 (t, J=7.0 Hz, 2H), 3.1-3.0 (m, 4H), 2.1 (m, 2H), 1.9 (m, 2H), 1.1 (t, J=7.6 Hz, 3H); m/z (APCI-neg) M−1=452.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394795B2
Source datasetuspto-grants-2013_03
ORD IDord-8fb185360e5a4793b60e30bbc7a97f11
Source noteuspto-grants-2013_03