HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646957Generated: November 1, 2026
Methyl p-toluenesulfonate → HCID 19800195, compound
https://huagongshe.com/reaction/1646957
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | HCID 19800209 | HCID 19800209 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19800195 | HCID 19800195 | 25.1% |
Reaction Steps
Add 1,3-dihydro-N-phenyl-3-(phenylthio)-2H-pyrrolo(2,3-b)pyridine (4.0 g, 12.6 mmole) portionwise to potassium hydride (KH) (1.73 g of 35 weight-percent KH in oil, washed with hexane, 15.1 mmole) in dry DMF (50 mL) at 0° C. under a nitrogen atmosphere. Stir for 45 minutes at 0° C. Add methyl tosylate(3.04 g, 16.3 mmole), and warm the reaction mixture up to room temperature slowly. Stir for 16 hours at room temperature. Remove DMF by high vacuum distillation. Add saturated aqueous NH4Cl (150 mL) and extract with ethyl acetate. Wash the organic extracts with saturated aqueous NaCl, dry with MgSO4, filter and rotoevaporate to give an oil. Dissolve oil in dichloromethane and chromatograph on silica gel, eluting with ethyl acetate:hexane (1:6). Combine appropriate fractions and concentrate under reduced pressure to give an oil. Crystallize the oil with diethyl ether-hexane to give the title compound as a white solid (1.05 g, m.p.=86°-87.5° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05182289 |
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| Source dataset | uspto-grants-1993_01 |
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| ORD ID | ord-40a45035b78c4cc0957c8418643c975b |
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| Source note | uspto-grants-1993_01 |
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