HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750139Generated: October 28, 2026
Sodium Iodide → 5-(3-(4-(2,3-dichlorophenyl)piperazin-1-yl)propoxy)-1H-benzo[d]imidazol-2(3H)-one
https://huagongshe.com/reaction/1750139
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(2,3-Dichlorophenyl)piperazine hydrochloride | HCID 11630372 | — |
| Reactant | 5-(3-bromopropoxy)-1H-benzo[d]imidazol-2(3H)-one | HCID 66633688 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-(3-(4-(2,3-dichlorophenyl)piperazin-1-yl)propoxy)-1H-benzo[d]imidazol-2(3H)-one | HCID 56597094 | 27.3% |
Reaction Steps
A mixture of intermediate 39 (126 mg, 0.47 mmol) and NaI (140 mg, 0.93 mmol) in CH3CN was heated to reflux for 30 min and then cooled to rt. Intermediate 41 (188 mg, 0.71 mmol) and anhydrous K2CO3 (259 mg, 1.88 mmol) were added to the mixture. The resulting mixture was heated to reflux and stirred overnight. Precipitated crystals were filtered off and the filtrate was evaporated under reduced pressure. The residue was extracted with EtOAc. The combined EtOAc layers were washed with brine, dried over anhydrous Na2SO4, concentrated in vacuo and purified by flash chromatography on silica gel column (elution with DCM/MeOH=15:1) to give 5-(3-(4-(2,3-dichlorophenyl)piperazin-1-yl)propoxy)-1H-benzo[d]imidazol-2(3H)-one (compound 34) (54 mg, 27%). 1H NMR (300 MHz, DMSO): δ 10.60 (s, 1H), 10.36 (s, 1H), 7.32 (d, J=5.1 Hz, 2H), 7.16-7.18 (m, 1H), 6.80 (d, J=9.6 Hz, 1H), 6.51-6.53 (d, J=6.6 Hz, 2H), 3.99-3.95 (m, 2H), 2.81-3.26 (s, 5H), 2.80-2.60 (m, 5H), 1.80-2.01 (m, 2H). HPLC: 99%, RT 2.228 min. MS (ESI) m/z 421.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156822B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-8051285f56ee4a39836fe5a5ee30e7fb |
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| Source note | uspto-grants-2015_10 |
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