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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 907337Erstellt: 25. Oktober 2026

Hydrochloric Acid → HCID 25020401, Verbindung

https://huagongshe.com/reaction/907337

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium cyanoborohydrideHCID 5003444—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukttert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 24820294—
EduktN-Cyclopropyl-3-(2-(cyclopropylmethyl)-4-formyl-1-oxo-1,2-dihydroisoquinolin-6-yl)-5-fluoro-4-methylbenzamideHCID 57551841—
KatalysatorAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktHCID 25020401HCID 25020401—

Reaktionsschritte

The product of Example 75 step i) (0.4 g), (S)-3-hydroxymethyl-piperazine-1-carboxylic acid, tert-butyl ester (0.83 g) and sodium triacetoxyborohydride (0.81 g) were stirred in dichloromethane (20 mL) at room temperature for 12 hours. A few drops of acetic acid were added and stirring continued for 12 hours. Methanol (10 ml) and sodium cyanoborohydride (0.70 g) were added and stirring continued for a further 12 hours. Methanol (10 ml) and 4M HCl in 1,4-dioxane (10 ml) were added and stirred for 12 hours. The volatiles were removed under vacuum, dilute aqueous ammonia was added and the mixture extracted into dichloromethane. The organics were combined and evaporated under reduced pressure. The residue was purified by HPLC to give the title compound (0.035 g) as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08012979B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-e0d336717db14615b82301be90259508
Quellennotizuspto-grants-2011_09