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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 69884Erstellt: 24. Oktober 2026

3-Amino-6-bromopyrazine-2-carboxylic acid → Tert-butyl 1-(2-(3-amino-6-bromopyrazine-2-carboxamido)-4-methoxyphenyl)piperidin-4-ylcarbamate

https://huagongshe.com/de/reaction/69884

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Amino-6-bromopyrazine-2-carboxylic acidHCID 18521600—
EduktHCID 69043362HCID 69043362—
LösungsmittelAcetonitrileHCID 6342—
ProduktTert-butyl 1-(2-(3-amino-6-bromopyrazine-2-carboxamido)-4-methoxyphenyl)piperidin-4-ylcarbamateHCID 866691837%

Reaktionsschritte

Following method 11, tert-butyl 1-(2-amino-4-methoxyphenyl)piperidin-4-ylcarbamate was coupled to 3-amino-6-bromopyrazine-2-carboxylic acid with TEA (3 eq) in ACN at 55° C. for 48 hours. Concentrated, triturated in cold ACN, filtered, and dried in vacuo yielding tert-butyl 1-(2-(3-amino-6-bromopyrazine-2-carboxamido)-4-methoxyphenyl)piperidin-4-ylcarbamate (7%). LCMS (m/z): 521.1 (MH+); LC Rt=3.63 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822497B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-ad9762d1a2d848578ffc5fb59556b8ac
Quellennotizuspto-grants-2014_09