Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 17895683 | HCID 17895683 | — |
| Reactant | HCID 68630196 | HCID 68630196 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 56597090 | HCID 56597090 | 82.7% |
Reaction Steps
A mixture of intermediate 26 (114 mg, 0.4 mmol) and NaI (120 mg, 0.8 mmol) in CH3CN was heated to reflux for 30 min and then cooled to rt. Intermediate 47 (160 mg, 0.6 mmol) and anhydrous K2CO3 (221 mg, 1.6 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-(4-(4-(2,3-dichlorophenyl)piperidin-1-yl)butoxy)benzo[d]thiazole (compound 21) (144 mg, 66%). 1H NMR (300 MHz, CDCl3): δ 8.97 (s, 1H), 7.80 (d, J=8.7 Hz, 1H), 7.61 (d, J=2.1 Hz, 1H), 7.33-7.29 (m, 1H), 7.26-7.16 (m, 1H), 7.09 (dd, J=2.1 Hz, 8.7 Hz, 3H), 4.10 (t, J=6.6 Hz, 2H), 3.13-3.09 (m, 2H), 2.50 (t, J=7.5 Hz, 2H), 2.14-2.10 (m, 2H), 1.91-1.74 (m, 10H). HPLC: 99%, RT 2.689 min. MS (ESI) m/z 435.3 [M+H]+. mp: 79-81° 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-01f5e4e0717d4949b9a80edfccb361a2 |
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| Source note | uspto-grants-2015_10 |
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