HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352232Generated: November 2, 2026
Benzenesulfonyl chloride → HCID 22149018, compound
https://huagongshe.com/reaction/1352232
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | HCID 22149012 | HCID 22149012 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22149018 | HCID 22149018 | — |
Reaction Steps
A mixture of N-(t-butoxycarbonyl)-2-(6H-thieno[2,3-b]pyrrol-4-yl)ethylamine (54 mg, 0.2 mmol), phenylsulfonyl chloride (70 mg, 0.22 mmol) and KOt-Bu (0.22 mL 1 M solution in THF, 0.22 mmol) in THF is shaken at ambient temperatures for 8 h and concentrated in vacuo. The resultant residue is dissolved in THF, treated with 4N HCl in dioxane (2 mL) shaken at room temperature for 16 h and concentrated in vacuo. This residue is dissolved in a mixture of DMSO, methanol and water and purified by preparative HPLC1, to afford the title product, [M+H]307, retention time (RT) 1.53 min. 1 Gilson Preparative HPLC conditions: Gilson Preparative HPLC system; YMC Pro-C18, 20 mm×50 mm ID, 5 uM column; 2 mL injection; Solvent A: 0.02% TFA/water; Solvent B:0.02% TFA/acetonitrile; Gradient: Time 0: 95% A; 2 min: 95% A; 14 min: 10% A, 15 min: 10% A, 16 min: 95% A; Flow rate 22.5 mL/min; Detection: 254 nm DAD.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07220756B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-9404775945594e38ae940fa50a3f6d8e |
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| Source note | uspto-grants-2007_05 |
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