HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50037Generated: October 29, 2026
HCID 131724381, compound → HCID 131724380, compound
https://huagongshe.com/reaction/50037
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 131724381 | HCID 131724381 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131724380 | HCID 131724380 | 100% |
Reaction Steps
A solution of 5-nitro-3-(3,5-dimethylphenylsulfonyl)indole-2-carboxyamide (5k) (0.25 g, 0.0007 mol) in tetrahydrofuran (40 ML) and methanol (16 mL) was reduced under an atmospheric pressure of hydrogen in the presence of PtO2 (50 mg) as a catalyst for 6 hours. Catalyst was separated by filtration and the solvent evaporated to give 0.227 g (100%) of pure 5-amino-3-(3,5-dimethylphenylsulfonyl)indole-2-carboxyamide as a brown oil. A solution of the last compound (0.227 g, 0.0007 mol), 2,5-dimethoxythetrahydrofuran (0.09 g, 0.0006 mol) in glacial acetic acid (5 mL) was refluxed for 30 minutes. After evaporation of the solvent the residue was triturated with ice water and extracted with ethyl acetate. Organic layer was washed with brine and dried. Removal of the solvent left the crude product which was purified by passing through a silica gel column chromatography (ethyl acetate as eluent) to give 0.15 g (57%) of title compound, mp 270-272° C. (from ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06710068B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-6fc9f567ff8541458a62a62b7296cae3 |
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| Source note | uspto-grants-2004_03 |
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