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HRID 330605作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Aspidospermidine-3-carboxylic acid, 4-(acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-, methyl ester, (2beta,3beta,4beta,5alpha,12beta,19alpha)-HCID 16596—
反応物Tert-Butyl hypochloriteHCID 521297—
反応物Potassium borohydrideHCID 4192641—
反応物HCID 178524011HCID 178524011—
触媒Silver tetrafluoroborateHCID 159722—
溶媒Acetic AcidHCID 176—
溶媒AcetoneHCID 180—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物Indole dihydroindoleHCID 19849603—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04897477
出典データセットuspto-grants-1990_01
ORD IDord-e422f63df0ed42bbb2bac7429a9e6d49
出典メモuspto-grants-1990_01