HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602508Generated: October 30, 2026
Ammonium Chloride → HCID 178441410, compound
https://huagongshe.com/reaction/1602508
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | HCID 19611382 | HCID 19611382 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178441410 | HCID 178441410 | 74% |
Reaction Steps
Dimethylformamide (13 ml) was added to a mixture of 3-[(4-tert-butyl-2-thiazolyl)methoxy]-5'-[3-(4-chlorophenylsulfonyl)propyl]-2'-cyanomethoxybenzanilide (1.30 g, 2.04 mmol), ammonium chloride (0.20 g, 4.08 mmol) and sodium azide (0.25 g, 4.08 mmol), and the resulting mixture was stirred at 70° C. for 12 hours. Ice and 5% sodium hydrogensulfate aqueous solution were added to the reaction solution and the product formed was extracted with ethyl acetate. The resulting organic layer was washed with water and brine in that order, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. Thereafter, the resulting residue was purified by silica gel column chromatography (eluent=methanol:chloroform=5:100) and then crystallized from acetonitrile to give 3-[(4-tert-butyl-2-thiazolyl)methoxy]-5'-[3-(4-chlorophenylsulfonyl)propyl]-2'-(1H-tetrazol-5-ylmethoxy)benzanilide (1.02 g, 74%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05981559 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-2f4aee6251694bf883014b827b5c5560 |
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| Source note | uspto-grants-1999_11 |
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