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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216942Erstellt: 27. Oktober 2026

Methyl N-(triethylammoniosulfonyl)carbamate → (S)-tert-Butyl 4-(1-cyano-2-(4-(3-methyl-2-oxo-2,3-dihydrobenzo[d]oxazol-5-yl)phenyl)ethylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate

https://huagongshe.com/reaction/216942

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl N-(triethylammoniosulfonyl)carbamateHCID 2724994—
Edukt(S)-tert-Butyl 4-(1-amino-3-(4-(3-methyl-2-oxo-2,3-dihydrobenzo[d]oxazol-5-yl)phenyl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 59568600—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-tert-Butyl 4-(1-cyano-2-(4-(3-methyl-2-oxo-2,3-dihydrobenzo[d]oxazol-5-yl)phenyl)ethylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamateHCID 59568548—

Reaktionsschritte

(S)-tert-Butyl 4-(1-amino-3-(4-(3-methyl-2-oxo-2,3-dihydrobenzo[d]oxazol-5-yl)phenyl)-1-oxopropan-2-ylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate (Example 17, step (i), 150 mg) in dichloromethane (15 mL) was treated with Burgess' reagent (100 mg) and stirred for 18 h. The reaction mixture was evaporated to a residue (145 mg) and used crude in the following step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193239B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-1d2f6cea69a64fc6af74d059e8bfd60e
Quellennotizuspto-grants-2012_06