HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398673Generated: October 29, 2026
Ammonium Chloride → 2-(3-Amino-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acid methyl ester
https://huagongshe.com/reaction/398673
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-propionic acid methyl ester | HCID 12069507 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(3-Amino-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acid methyl ester | HCID 54438541 | 108.5% |
Reaction Steps
A solution of 3-cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-propionic acid methyl ester (prepared as in Example 14, 1.50 g, 4.22 mmol) in methanol (30 mL) was treated with a solution of ammonium chloride (474 mg, 8.86 mmol) in water (3 mL). The reaction mixture was stirred at 25° C. for 5 min and then treated with zinc dust (2.70 g, 41.36 mmol). The reaction mixture was heated under reflux for 2 h. The reaction mixture was allowed to cool to 25° C. and then filtered through a pad of celite. The filtrate was concentrated in vacuo. The resulting orange oil was dissolved in ethyl acetate, dried over magnesium sulfate, filtrated, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 2/1 hexanes/ethyl acetate) afforded 2-(3-amino-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acid methyl ester (1.49 g, 98%) as a white solid: mp 98-100° C.; EI-HRMS m/e calcd for C16H23NO4S (M+) 325.1348, found 325.1358.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610846B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-9df76e09b833493caa6aebf72ba663a2 |
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| Source note | uspto-grants-2003_08 |
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