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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 330605Erstellt: 25. Oktober 2026

Aspidospermidine-3-carboxylic acid, 4-(acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-, methyl ester, (2beta,3beta,4beta,5alpha,12beta,19alpha)- → Indole dihydroindole

https://huagongshe.com/reaction/330605

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAspidospermidine-3-carboxylic acid, 4-(acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-, methyl ester, (2beta,3beta,4beta,5alpha,12beta,19alpha)-HCID 16596—
EduktTert-Butyl hypochloriteHCID 521297—
EduktPotassium borohydrideHCID 4192641—
EduktHCID 178524011HCID 178524011—
KatalysatorSilver tetrafluoroborateHCID 159722—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelAcetoneHCID 180—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
ProduktIndole dihydroindoleHCID 19849603—

Reaktionsschritte

Using the procedure of Example 25, 0.522 g (0.887 mmol) of 4,2'-PARF methyl 3-benzyl-1,2,3,3a,4,5-hexahydro-4-[2-p-toluenesulfonyloxymethyl) propyl]-7H-pyrrolo (2,3-d)-carbazole-6-carboxylate on reaction with 0.141 g (1.29 mmol) of t-butyl hypochlorite and 0.136 g ((0.187 mL) of triethylamine in 25 mL of dichloromethane, followed by a reaction with 0.297 g (0.654 mmol) of vindoline, 0.204 g (1.29 g mmol) of tetrafluoroboric acid diethyl ether complex and 0.245 g (1.26 mmol) of silver tetrafluoroborate in 6 mL of acetone, followed by reduction with 0.453 g (8.42 mmol) of potassium borohydride in 15 mL of acetic acid gave 0.276 g (41%) of the more polar 7R indole-indoline product, eluted on centrifugal chromatography with ether/acetone/triethylamine, 100:20:2, and 0.264 g (39%) of the less polar 7S indole-indoline product, eluted with ethyl acetate/ethanol/triethylamine 95:5:1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04897477
Quelldatensatzuspto-grants-1990_01
ORD IDord-e422f63df0ed42bbb2bac7429a9e6d49
Quellennotizuspto-grants-1990_01