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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 633812Erstellt: 25. Oktober 2026

Acetic Acid → HCID 178487803, Verbindung

https://huagongshe.com/reaction/633812

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carbaldehydeHCID 10773638—
EduktHCID 178487802HCID 178487802—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelMethanolHCID 887—
ProduktHCID 178487803HCID 178487803—

Reaktionsschritte

3-Oxo-3,4-dihydro-2H-benzo[1,4]oxazine-6-carbaldehyde (27 mg, 0.14 mmol, 1.0 eq) is added at room temperature to a stirred solution of trans-4-(8-methoxy-1,2-dihydro-3-oxa-5,9-diaza-cyclopenta[a]naphthalen-2-ylmethyl)-cyclohexylamine (47 mg, 0.14 mmol, 1.0 eq) in 1,2-dichloroethane (4 mL) and methanol (1 mL), followed by acetic acid (11 μL, 0.19 mmol, 1.3 eq) and sodium cyanoborohydride (11 mg, 0.16 mmol, 1.15 eq). After 5 hours stirring at room temperature, the reaction mixture is extracted with dichloromethane (3×10 mL) and a saturated sodium hydrogen carbonate aqueous solution (10 mL). The combined organic layers are dried over sodium sulfate, filtered and concentrated to give a residue that is purified by preparative HPLC to afford 6-{[trans-4-(8-methoxy-1,2-dihydro-3-oxa-5,9-diaza-cyclopenta[a]naphthalen-2-ylmethyl)-cyclohexylamino]-methyl}-4H-benzo[1,4]oxazin-3-one as a white lyophilized powder (13 mg, 18% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09321788B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-31ffafcb6de2464d9a8b70da9be520de
Quellennotizuspto-grants-2016_04