HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609393Generated: November 1, 2026
p-Toluenesulfonic acid → 1H-Pyrrole-2,5-dione, 3,4-bis(1-methyl-1H-indol-3-yl)-
https://huagongshe.com/reaction/1609393
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-Methyl-3-indoleglyoxylic acid | HCID 4589028 | — |
| Reactant | Isopropyl 1-methyl-3-indoleacetimidate hydrochloride | HCID 22907276 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1H-Pyrrole-2,5-dione, 3,4-bis(1-methyl-1H-indol-3-yl)- | HCID 5327655 | 30% |
Reaction Steps
A stirred solution of 406 mg (2 mmol) of 1-methyl-3-indolylglyoxylic acid in 20ml of dichloromethane was treated with 202 mg (2 mmol) of triethylamine and 273 mg (2 mmol) of isobutyl chloroformate. After 0.5 hour, the solution was added dropwise to a stirred solution of 533 mg (2 mmol) of isopropyl 1-methyl-3-indoleacetimidate hydrochloride and 808 mg (8 mmol) of triethylamine in 50 ml of dichloromethane. The solution obtained was heated to reflux under nitrogen for 18 hours, cooled and treated with 1.9 g (10 mmol) of p-toluenesulfonic acid. After 1 hour, the solvent was removed under reduced pressure and the residue was purified by flash chromatography on silica gel using dichloromethane/ethyl acetate (8:1) for the elution to give 107 mg(30% ) of 3,4-bis-(1 -methyl-3-indolyl)-1H-pyrrole-2,5-dione in the form of an orange colored solid of melting point >310° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05399712 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-596341b7a3734edf99bc8fea3d8c8aed |
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| Source note | uspto-grants-1995_03 |
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