HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943877Generated: November 2, 2026
Tetrabutylammonium Fluoride → HCID 178461061, compound
https://huagongshe.com/reaction/1943877
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 178461062 | HCID 178461062 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178461061 | HCID 178461061 | 52% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08394795B2 |
|---|
| Source dataset | uspto-grants-2013_03 |
|---|
| ORD ID | ord-8fb185360e5a4793b60e30bbc7a97f11 |
|---|
| Source note | uspto-grants-2013_03 |
|---|