HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750122Generated: October 28, 2026
Sodium Iodide → 5-(3-(4-(2,3-Dichlorophenyl)piperazin-1-yl)propoxy)benzo[d]thiazole
https://huagongshe.com/reaction/1750122
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)benzo[d]thiazole | HCID 66631551 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-(3-(4-(2,3-Dichlorophenyl)piperazin-1-yl)propoxy)benzo[d]thiazole | HCID 56599143 | 62% |
Reaction Steps
A mixture of intermediate 27 (218 mg, 0.8 mmol) and NaI (240 mg, 1.6 mmol) in CH3CN was heated to reflux for 30 min and then cooled to rt. Intermediate 41 (320 mg, 1.2 mmol) and anhydrous K2CO3 (442 mg, 3.2 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=30:1) to give 5-(3-(4-(2,3-dichlorophenyl)piperazin-1-yl)propoxy)benzo[d]thiazole (compound 23) (209 mg, 62%). 1H NMR (300 MHz, CDCl3): δ 8.97 (s, 1H), 7.80 (d, J=8.7 Hz, 1H), 7.63 (d, J=2.1 Hz, 1H), 7.16-7.09 (m, 3H), 6.94 (dd, J=3.6 Hz, 6.0 Hz, 1H), J=5.7 Hz, 2H), 3.09 (m, 4H), 2.68-2.63 (m, 6H), 2.10-2.05 (m, 2H). HPLC: 99%, RT 2.607 min. MS (ESI) m/z 422.0 [M+H]+. mp: 127-129° C.
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-11b8a1b18ff7451892dfe150a1582b59 |
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| Source note | uspto-grants-2015_10 |
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