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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256282Generated: October 30, 2026

Phosphate → HCID 86652263, compound

https://huagongshe.com/reaction/1256282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 86652264HCID 86652264—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86652263HCID 86652263—

Reaction Steps

4-(1-(tert-Butyldimethylsilyloxy)-2-methylpropan-2-yl)-N-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)benzamide (4F, 3.9 g, 1.0 equivalent) was dissolved in THF (0.13 M) and treated with TBAF (1.0 M in THF, 4.0 equivalents). After 60 hours, pH 7 phosphate buffer was added and the mixture was extracted with EtOAc. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by chromatography (SiO2, gradient of 25 to 50% EtOAc/hexanes) to give N-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(1-hydroxy-2-methylpropan-2-yl)benzamide (4G) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.25 (s, 6 H), 2.44 (s, 3 H), 3.46 (d, J=5.05 Hz, 2 H), 4.76 (t, J=5.31 Hz, 1 H), 6.45 (s, 1 H), 7.52 (d, J=8.59 Hz, 2 H), 7.99 (d, J=8.59 Hz, 2 H), 8.06 (s, 1 H), 11.30 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461163B2
Source datasetuspto-grants-2013_06
ORD IDord-d73906e372e44abeb342a73fa55f4c91
Source noteuspto-grants-2013_06