HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640972Generated: October 26, 2026
4-(2-(Pyrrolidin-1-yl)ethyl)aniline → HCID 178426937, compound
https://huagongshe.com/reaction/640972
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(2-(Pyrrolidin-1-yl)ethyl)aniline | HCID 6487047 | — |
| Reactant | HCID 178426964 | HCID 178426964 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178426937 | HCID 178426937 | 41% |
Reaction Steps
was charged with 2,5-Dimethyl-2H-pyrazole-3-carboxylic acid [3-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (as prepared in Example 60, 100 mg, 0.249 mmol) and THF (2 mL). To the resulting solution was added 4-(2-Pyrrolidin-1-yl-ethyl)-phenylamine (47.3 mg, 0.249 mmol), and the mixture was stirred for 24 h at 65° C. The reaction mixture was cooled to room temperature. Hexanes were added to the reaction mixture causing a black precipitate to form. The precipitate was vacuum filtered and the filtrate was then concentrated in vacuo and redissolved into ˜3 mL of EtOAc. Hexanes were added causing a yellow precipitate to form. The precipitate was then filtered and washed with ˜1 mL of i-prOH yielding 41% (0.058 g, 0.102 mmol) of the title compound.
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-ec5d537771a14770a3f6557e9bd156e7 |
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| Source note | uspto-grants-2010_04 |
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