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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10987Erstellt: 23. Oktober 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → CID 145857197

https://huagongshe.com/de/reaction/10987

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
EduktHOAtHCID 181649—
EduktSodium BicarbonateHCID 516892—
Edukt(S)-3-{[(benzyloxy)carbonyl][3-(trifluoromethyl)benzyl]amino}-4-oxo-4,6,7,8-tetrahydropyrrolo[1,2-a]pyrimidine-6-carboxylic AcidHCID 57444827—
Edukttert-butyl N-[4-(aminomethyl)benzenecarboximidoyl]carbamateHCID 145832046—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmitteldichloromethane N,N-dimethylformamideHCID 22350042—
ProduktCID 145857197HCID 14585719779,2%

Reaktionsschritte

To a solution of intermediate 25a (0.281 mmol) and [(4-aminomethyl-phenyl)-imino-methyl]-carbamic acid tert-butyl ester (84 mg, 0.337 mmol) in 3 mL 5:1 CH2Cl2/DMF at 0° C., were added NaHCO3 (59 mg, 0.703 mmol), HOAT (42.1 mg, 0.309 mmol), and EDCI (75.5 mg, 0.393 mmol). The mixture was allowed to warm to rt and stir 20 h, then was diluted with EtOAc. The organic phase was washed with H2O, 1N HCl, H2O, and sat. NaHCO3, and brine, dried (Na2SO4) and brine. The crude residue was triturated with Et2O to afford 160 mg (79%) of intermediate 25b as a white solid. MS (ESI) 719.4 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094783B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-f36da15899fd4af9811f6c580396af9c
Quellennotizuspto-grants-2006_08