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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330605Generated: October 26, 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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAspidospermidine-3-carboxylic acid, 4-(acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-, methyl ester, (2beta,3beta,4beta,5alpha,12beta,19alpha)-HCID 16596—
ReactantTert-Butyl hypochloriteHCID 521297—
ReactantPotassium borohydrideHCID 4192641—
ReactantHCID 178524011HCID 178524011—
CatalystSilver tetrafluoroborateHCID 159722—
SolventAcetic AcidHCID 176—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductIndole dihydroindoleHCID 19849603—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04897477
Source datasetuspto-grants-1990_01
ORD IDord-e422f63df0ed42bbb2bac7429a9e6d49
Source noteuspto-grants-1990_01