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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442754Generated: November 2, 2026

Hydrochloric Acid → HCID 53730750, compound

https://huagongshe.com/reaction/442754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 54159292HCID 54159292—
SolventWaterHCID 962—
ProductHCID 53730750HCID 53730750—

Reaction Steps

3-(6-hydroxy-1-methyl-1H-indol-3-yl)-4-(1-methyl-1H-indol-3-yl)-pyrrole-2,5-dione was prepared by treating Benzenesulfonic acid 1-methyl-3-[4-(1-methyl-1H-indol-3-yl)-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl]-1H-indol-6-yl ester (141 mg 0.28 mm) with 4N NaOH (0.5 mL, 2 mmol) and CH3OH (4 mL) and heating to reflux temperature for 6 hours. After cooling to room temperature, the reaction mixture was diluted with H2O, acidified with 2N HCl, and extracted with EtOAc. The organic phase was washed with saturated NaCl solution, dried over MgSO4, filtered and evaporated to afford, after purification by flash column chromatography 3-(6-hydroxy-1-methyl-1H-indol-3-yl)-4-(1-methyl-1H-indol-3-yl)-pyrrole-2,5-dione (15 mg); mp=279°-282° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891901
Source datasetuspto-grants-1999_04
ORD IDord-6de721acca244f0e8d4a2e1c48334d5b
Source noteuspto-grants-1999_04