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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 334003Erstellt: 26. Oktober 2026

Phenethylamine → 1307953-73-6

https://huagongshe.com/reaction/334003

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenethylamineHCID 1001—
EduktN-Cbz-d-alanineHCID 70832—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
EduktIsoquinoline-6-sulfonyl chlorideHCID 55280287—
KatalysatorHCID 178418390HCID 178418390—
LösungsmittelDichloromethaneHCID 6344—
Produkt1307953-73-6HCID 1091378845,7%

Reaktionsschritte

Phenethylamine (285 mg) and N-(benzyloxycarbonyl)-D-alanine (500 mg) were condensed (618 mg, 85%) using 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (472 mg) in dichloromethane. (R)-2-amino-N-phenethylpropanamide (197 mg) obtained by further hydrogenation reaction in the presence of 10% palladium-carbon, and isoquinoline-6-sulfonyl chloride prepared in Reference Example 1 were condensed (237 mg, 60%) in the presence of triethylamine (0.284 mL) in dichloromethane. Subsequently, 40 mg of the title compound was obtained as a pale yellow solid (13%) with reference to the method of Step 3 of Example 1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08883792B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-80a3c77f7b164a1d9c7b22b5197614d3
Quellennotizuspto-grants-2014_11