HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 383122Erstellt: 26. Oktober 2026
Acetic Acid → {4-[(2S,4R)-1-Boc-4-(t-butyldimetylsilyl)oxypyrrolidin-2-ylmethyl]amino-2-phenylbenzoyl}methionine methyl ester
https://huagongshe.com/reaction/383122
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Edukt | tert-Butyl (2S,4R)-4-((tert-butyldimethylsilyl)oxy)-2-formylpyrrolidine-1-carboxylate | HCID 10969557 | — |
| Edukt | N-(4-Amino-2-phenylbenzoyl)methionine methyl ester | HCID 18666758 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | {4-[(2S,4R)-1-Boc-4-(t-butyldimetylsilyl)oxypyrrolidin-2-ylmethyl]amino-2-phenylbenzoyl}methionine methyl ester | HCID 70213927 | 74% |
Reaktionsschritte
To a solution of 0.75 g (2.09 mmol) of [2-phenyl-4-aminobenzoyl]methionine methyl ester (compound 8) and 0.7 g (2.1 mmol) of (2S,4R)-1-Boc-4-[t-butyldimethylsilyloxy]-pyrrolidin-2-aldehyde, prepared as in Example 171B, in 10 ml of methanol were added 1 ml of acetic acid, followed by 0.2 g (3.1 mmol) of sodium cyanoborohydride. The reaction mixture was stirred overnight. After removal of the solvent, the residue was partitioned with ethyl acetate and 5% sodium bicarbonate, and extracted 3 times with ethyl acetate. The combined organic solution was washed with water and brine, dried over magnesium sulfate, and solvent was removed. The residue was flash-chromatographed on silica gel (2:1 hexanes-ethyl acetate) to yield 261 mg (74%) of {4-[(2S,4R)-1-Boc-4-(t-butyldimetylsilyl)oxypyrrolidin-2-ylmethyl]amino-2-phenylbenzoyl}methionine methyl ester as a white solid: mp 48° C.; [α]25D−15.6 (c=1.03, CHCl3);
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06310095B1 |
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| Quelldatensatz | uspto-grants-2001_10 |
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| ORD ID | ord-8fda9393fddd4117b1770a43cd252330 |
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| Quellennotiz | uspto-grants-2001_10 |
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