HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215108Generated: November 2, 2026
Hydrochloric Acid → HCID 178527343, compound
https://huagongshe.com/reaction/2215108
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 68570377 | HCID 68570377 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178527343 | HCID 178527343 | — |
Reaction Steps
1 M NaOH solution (0.63 mmol, 1.0 eq) is added to a stirred solution of 2,4-dichloro-N-[1-(2-cyano-ethyl)-1H-tetrazol-5-ylmethyl]-N-[2-(indan-5-yloxy)-ethyl]benzene sulfonamide (0.325 g, 1 eq.) in tetrahydrofuran (3 ml) at room temperature and the reaction mixture stirred overnight. The reaction mixture is acidified with 1 M HCl solution to pH 3, and then extracted with EtOAc (20 ml). The organic extract is washed with 1 M HCl solution (2×5 ml), and then with brine (1×10 ml), dried over MgSO4, and concentrated to give a crude solid (0.211 g), which is triturated with Et2O, filtered, washed with Et2O and dried under suction. The solid is purified by preparative HPLC to give pure 2,4-dichloro-N-[2-(indan-5-yloxy)-ethyl]-N-(1H-tetrazol-5-ylmethyl)benzene-sulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109203B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-4175f4f35a6140d1a2e366a75327e879 |
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| Source note | uspto-grants-2006_09 |
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