HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166191Generated: November 2, 2026
Benzenesulfonyl chloride → HCID 12085355, compound
https://huagongshe.com/reaction/1166191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 12085354 | HCID 12085354 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12085355 | HCID 12085355 | — |
Reaction Steps
A stirred solution of tert-butyl 5-[(5-fluoro-1H-indol-3-yl)methyl]-3,6-dihydro-1(2H)-pyridinecarboxylate (430 mg, 1.30 mmol) in tetrahydrofuran is treated with NaH (60% in mineral oil, 78 mg, 1.95 mmol) portion-wise under nitrogen at room temperature, stirred for 0.5 hr, treated with benzenesulfonyl chloride (0.25 ml, 1.95 mmol), stirred for 17 hr under nitrogen at room temperature, quenched with ice-water and diluted with ethyl acetate. The phases are separated and the aqueous phase is extracted with ethyl acetate. The combined extracts and organic phase are washed with water and saturated NaCl, dried over MgSO4 and concentrated in vacuo. The resultant residue is purified by flash chromatography (silica gel, EtOAc/hexane, 1/9) to afford the title compound as a yellow solid, 350 mg, mp 63-65° C., identified by NMR and mass spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06613781B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-3d07f12a7b644716b0349328659bd029 |
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| Source note | uspto-grants-2003_09 |
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