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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216930Erstellt: 25. Oktober 2026

Methyl N-(triethylammoniosulfonyl)carbamate → (S)-tert-Butyl 4-(1-cyano-2-(4-(4-methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)phenyl)ethylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate

https://huagongshe.com/reaction/216930

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl N-(triethylammoniosulfonyl)carbamateHCID 2724994—
Edukt(S)-tert-Butyl 4-(1-amino-3-(4-(4-methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)phenyl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 59568612—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-tert-Butyl 4-(1-cyano-2-(4-(4-methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)phenyl)ethylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 59568576104%

Reaktionsschritte

(S)-tert-Butyl 4-(1-amino-3-(4-(4-methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)phenyl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate (Example 10, step (iii), 155 mg) in dichloromethane (8 mL) was stirred at room temperature for 18 h with Burgess' reagent (134 mg). The solvent was partially evaporated and the mixture was absorbed onto silica for purification on a silica column using ethyl acetate/isohexane 1:1 as eluent to yield the sub-titled compound as a solid (156 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193239B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-bf0948e360df442aad8572b7cf7f8d11
Quellennotizuspto-grants-2012_06