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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 574355Erstellt: 24. Oktober 2026

Perchloric Acid → (S)-methyl 2-(2-bromo-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-(tert-butoxy)acetate

https://huagongshe.com/de/reaction/574355

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPerchloric AcidHCID 24247—
EduktSodium BicarbonateHCID 516892—
Edukt(S)-methyl 2-(2-bromo-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetateHCID 86695080—
LösungsmittelDichloromethaneHCID 6344—
Lösungsmitteltert-Butyl acetateHCID 10908—
Produkt(S)-methyl 2-(2-bromo-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-(tert-butoxy)acetateHCID 8669508186,8%

Reaktionsschritte

To a solution of (S)-methyl 2-(2-bromo-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate (5.68 g, 13.81 mmol, 1 equiv) in DCM (92 mL) and t-butyl acetate (184 mL) was added 70% perchloric acid (3.3 mL, 55.2 mmol, 4 equiv). The reaction turned pale yellow. After 3 h, the reaction was added very cautiously to a saturated aqueous solution of NaHCO3 and extracted with CHCl3 (×3). Combined organic extracts dried over Na2SO4 and concentrated in vacuo. The crude product was purified by silica gel flash chromatography (0-70% EtOAc/hexane) to provide (S)-methyl 2-(2-bromo-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-(tert-butoxy)acetate as a pale yellow solid (2.8 g, 43%) and recovered starting material (3.0 g, 53%). 1H NMR (400 MHz, CDCl3) δ 6.54 (s, 1H), 5.92 (s, 1H), 3.74 (s, 3H), 2.59 (s, 3H), 1.58 (s, 8H), 1.24 (s, 9H), 1.11 (s, 6H); LCMS (ESI, M+1):467.3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09034882B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-f868f1ab2ec345dab43f8a5c615abaca
Quellennotizuspto-grants-2015_05