HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234363Generated: November 1, 2026
1-Pyrrolidineethanamine → HCID 57639973, compound
https://huagongshe.com/reaction/2234363
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Pyrrolidineethanamine | HCID 1344 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Fluoro-2-nitroanisole | HCID 2779250 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 57639973 | HCID 57639973 | 1.5% |
Reaction Steps
To a stirred solution of 4-fluoro-2-methoxy-1-nitro-benzene (Fluorochem; 2.57 g; 15 mmol) in DMA was 2-pyrrolidin-1-ylethanamine (Aldrich; 1.88 g, 16.5 mmol) followed by DIPEA (2.97 mL, 18 mmol). The mixture was heated at 80° C. for 20 hours, then cooled to room temp. The mixture was concentrated in vacuo, dissolved in DCM and purified by SCX (50 g SCX 2 column). The product was eluted from the column with 7N ammonia in methanol, concentrated in vacuo to give the title compound (53 mg) which was dissolved in Methanol as a 0.05 mmol solution and reduced using an H-cube hydrogenator. 10% Pd/C catalyst, 1 bar hydrogen (full hydrogen setting), 3 mL/min flow-rate at 50° C. The resultant solution was concentrated in vacuo, and the resultant material purified by column chromatography, eluting with 0-10% ammonia/methanol in DCM, to give the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07709471B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-5dcf8aeb8608405b975063335e78be7d |
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| Source note | uspto-grants-2010_05 |
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