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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216921Erstellt: 25. Oktober 2026

Methyl N-(triethylammoniosulfonyl)carbamate → (S)-tert-Butyl 4-(2-(4'-(azetidin-1-ylsulfonyl)biphenyl-4-yl)-1-cyanoethylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate

https://huagongshe.com/reaction/216921

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl N-(triethylammoniosulfonyl)carbamateHCID 2724994—
Edukt(S)-tert-Butyl 4-(1-amino-3-(4'-(azetidin-1-ylsulfonyl)biphenyl-4-yl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 70213622—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-tert-Butyl 4-(2-(4'-(azetidin-1-ylsulfonyl)biphenyl-4-yl)-1-cyanoethylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 7021121074,1%

Reaktionsschritte

(S)-tert-Butyl 4-(1-amino-3-(4′-(azetidin-1-ylsulfonyl)biphenyl-4-yl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate (Example 7, step (i), 309 mg) in dichloromethane (8 mL) was treated with Burgess' reagent (251 mg) and the mixture was stirred at room temperature for 18 h. The solvent was partially evaporated and then purified by chromatography on silica using diethyl ether and then 1:1 ethyl acetate/isohexane as eluent to yield a white solid (222 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193239B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-f0efc4c3558c48e1916dd659f8116b81
Quellennotizuspto-grants-2012_06