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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1371518Erstellt: 26. Oktober 2026

Sodium cyanoborohydride → tert-butyl 4-(2,3-dihydro-1H-indol-7-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1371518

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium cyanoborohydrideHCID 5003444—
Edukttert-butyl 4-(1H-indol-7-yl)piperazine-1-carboxylateHCID 21070951—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelSodium HydroxideHCID 14798—
Produkttert-butyl 4-(2,3-dihydro-1H-indol-7-yl)piperazine-1-carboxylateHCID 2107095046%

Reaktionsschritte

7-(4-t-Butyloxycarbonylpiperazin-1-yl)indole (200 mg, 0.67 mmol) is dissolved in acetic acid (4 mL). To the solution, sodium cyanoborohydride (84 mg, 1.33 mmol) is added. The reaction mixture is stirred for about 2 hours at r.t. The mixture is then diluted with DCM and NaOH (1M) is added. The organic layer is separated, dried and concentrated. The residue is chromatographed on the silica gel and the product containing fractions are combined to give about 93 mg of the 7-(4-t-butyloxycarbonylpiperazin-1-yl)-2,3-dihydroindole (46%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07157463B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-d0406b2b6c834bf7a4c9eaf99970312d
Quellennotizuspto-grants-2007_01