HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984537Generated: November 1, 2026
2-Dimethylaminopyridine → 1-[(5-Chlorothien-2-yl)sulfonyl]-3-[2-(dimethylamino)ethyl]-1,3-dihydro-2H-benzimidazol-2-one
https://huagongshe.com/reaction/1984537
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Chlorothiophene-2-sulfonyl chloride | HCID 2733925 | — |
| Reactant | 1-[2-(Dimethylamino)ethyl]-1,3-dihydrobenzimidazol-2-one | HCID 14894678 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[(5-Chlorothien-2-yl)sulfonyl]-3-[2-(dimethylamino)ethyl]-1,3-dihydro-2H-benzimidazol-2-one | HCID 11429094 | — |
Reaction Steps
A solution of 1-[2-(dimethylamino)ethyl]-1,3-dihydrobenzimidazol-2-one (20 mg, 0.1 mmol) in THF at room temperature is treated with (5-chlorothien-2-yl)sulfonyl chloride (26 mg, 0.12 mmol) followed by diisopropylethylamine (25 uL, 0.2 mmol) and dimethylaminopyridine (5 mg), stirred at room temperature for 16 hours and concentrated in vacuo. The resultant residue is dissolved in a mixture of dimethylsulfoxide, methanol and water and purified by Gilson1 preparative HPLC to give the title product, 16 mg, [M+H] 386, retention time (RT) 2.83 minutes. 1Gilson Preparative HPLC conditions: Gilson Preparative HPLC system; YMC Pro C18, 20 mm×50 mm ID, 5 uM column; 2 mL injection; Solvent A: 0.02% TFA/water; Solvent B:0.02% TFA/acetonitrile; Gradient: Time 0: 95% A; 2 min: 95% A; 14 min: 10% A, 15 min: 10% A, 16 min: 95% A; Flow rate 22.5 mL/min; Detection: 254 nm DAD.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07544701B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-b202429ebe3943e18864e1e2ed012ecb |
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| Source note | uspto-grants-2009_06 |
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