HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641018Generated: October 30, 2026
Tetrahydrofuran → 5-ethyl-1-methyl-N-[3-[2-oxo-3-[[4-(pyrrolidin-1-ylmethyl)anilino]methylidene]-1H-indole-6-carbonyl]phenyl]pyrazole-3-carboxamide
https://huagongshe.com/reaction/641018
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-(Pyrrolidin-1-ylmethyl)aniline | HCID 776852 | — |
| Reactant | 5-ethyl-N-[3-[3-(hydroxymethylidene)-2-oxo-1H-indole-6-carbonyl]phenyl]-1-methylpyrazole-3-carboxamide | HCID 178436688 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-ethyl-1-methyl-N-[3-[2-oxo-3-[[4-(pyrrolidin-1-ylmethyl)anilino]methylidene]-1H-indole-6-carbonyl]phenyl]pyrazole-3-carboxamide | HCID 178436686 | 18% |
Reaction Steps
A small screw cap test tube was charged with 5-Ethyl-1-methyl-1H-pyrazole-3-carboxylic acid [3-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (as prepared in Example 345, 70 mg, 0.1681 mmol) and THF (2.0 mL). To the resulting solution was added 4-Pyrrolidin-1-ylmethyl-phenylamine (30.1 mg, 0.171 mmol), and the mixture was stirred for 24 h at 65° C. Subsequently, the reaction mixture was cooled to room temperature and diluted with EtOAc (˜5 mL) and Hexane (˜40 mL). The solid that precipitated was collected by filtration and washed with 0° C. iPrOH (˜10 mL) affording the title compound in 18% yield (0.018 g, 0.031 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07692005B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-d6e4f936e9e040929d7eaf5f3c0d06f4 |
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| Source note | uspto-grants-2010_04 |
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