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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 430498Erstellt: 25. Oktober 2026

4-Methylmorpholine → N-[4-[(3-bromophenyl)amino]-6-quinazolinyl]-(3-phenyl-2-propynamide)

https://huagongshe.com/reaction/430498

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktIsobutyl chloroformateHCID 62365—
EduktPhenylpropiolic AcidHCID 69475—
EduktN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—
LösungsmittelPyridineHCID 1049—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-[4-[(3-bromophenyl)amino]-6-quinazolinyl]-(3-phenyl-2-propynamide)HCID 98462270,7%

Reaktionsschritte

A solution of 0.93 g of 3-phenyl-2-propynoic acid in 10 ml of tetrahydrofuran was cooled in an ice bath. A 0.82 ml portion of isobutyl chloroformate followed by a 0.69 ml portion of N-methyl morpholine were added. After about 1 minute a solution of 1.0 g of N-(3-bromophenyl)4,6-quinazolindiamine in 7 ml of pyridine was added. The reaction at 0° C. for 1 hr.. The solvents were removed at reduced pressure and the solid was purified by chromatography on silica gel to give 0.01 g of N-[4-[(3-bromophenyl)amino]-6-quinazolinyl]-(3-phenyl-2-propynamide): mass spectrum (m/e): 443.2, 445.2 (M+H, electrospray).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06323209B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-2b0269bb498842ba86a0ff757a966947
Quellennotizuspto-grants-2001_11