HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245378Generated: October 30, 2026
2-Methylpyrrolidine → HCID 87464554, compound
https://huagongshe.com/reaction/2245378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylpyrrolidine | HCID 13003 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 87464251 | HCID 87464251 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 87464554 | HCID 87464554 | — |
Reaction Steps
To a solution of 1-({[(2Z)-3-(2,2-difluoro-1,3-benzodioxol-5-yl)-5-methylene-1,3-thiazolidin-2-ylidene]amino}carbonyl)-3-methyl-1H-imidazol-3-ium iodide (Example 116, 0.1 g, 0.19 mmol) and 2-methylpyrrolidine (0.018 g, 0.19 mmol) in anhydrous acetonitrile (5 mL) was added Hunig's base (0.025 g), and then the solution was heated at 60° C. for 3 hours. After cooling to room temperature, the reaction was diluted with 50 mL of CH2Cl2, washed water and brine, dried over sodium sulfate, and evaporated under reduced pressure. The crude residue was choromatographed over silica using CH2Cl2 to give the titled compound. 1H NMR (CD3OD) δ ppm 1.00 (3H), 1.60 (1H), 1.90 (3H), 3.40 (2H), 3.90 (1H), 4.80 (2H), 5.20 (1H), 5.35 (1H), 7.30 (2H), 7.50 (1H); MS (ESI) 382(M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07683084B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-babb32854164460d82197e8dff6f6469 |
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| Source note | uspto-grants-2010_03 |
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