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HRID 390940Erstellt: 24. Oktober 2026

Trimethyl orthoformate → 2-Chloro-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)-4-morpholinofuro[3,2-d]pyrimidine

https://huagongshe.com/de/reaction/390940

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethyl orthoformateHCID 9005—
EduktSodium AcetateHCID 517045—
Edukt1-(Methylsulfonyl)piperazineHCID 709161—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt2-Chloro-4-morpholinofuro[3,2-d]pyrimidine-6-carbaldehydeHCID 56833742—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt2-Chloro-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)-4-morpholinofuro[3,2-d]pyrimidineHCID 5683374468%

Reaktionsschritte

2-Chloro-4-morpholinofuro[3,2-d]pyrimidine-6-carbaldehyde 39 prepared following Example 20 (65 mg, 1.0 eq) was dissolved in 1,2-dichloroethane (9.7 ml) and treated with hydrochloride salt of 1-methanesulfonylpiperazine (69 mg, 1.4 eq), sodium acetate (28 mg, 1.4 eq) and trimethyl orthoformate (0.27 ml, 10 eq). Reaction mixture was stirred at r.t. for 12 h. Sodium triacetoxyborohydride (62 mg, 1.2 eq) was added and reaction mixture was stirred at r.t. for 8 h. Reaction mixture was quenched with saturated aq. NaHCO3 and extracted with dichloromethane. The combined organic layers were dried (Na2SO4) and concentrated. The crude reaction mixture was purified by flash chromatography to yield 2-chloro-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)-4-morpholinofuro[3,2-d]pyrimidine (70 mg, 68%): MS (Q1) 416 (M)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383620B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-ccbfd02770054dbfb22ee0f1831f6b9e
Quellennotizuspto-grants-2013_02