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Chemical Structure| 161561-84-8 Chemical Structure| 161561-84-8

Structure of 161561-84-8

Chemical Structure| 161561-84-8

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Product Details of [ 161561-84-8 ]

CAS No. :161561-84-8
Formula : C9H18N2O4
M.W : 218.25
SMILES Code : O=C(OC(C)(C)C)N[C@@H](COC)C(N)=O

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Application In Synthesis of [ 161561-84-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 161561-84-8 ]

[ 161561-84-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 51293-47-1 ]
  • [ 161561-84-8 ]
YieldReaction ConditionsOperation in experiment
With pyridine; di-tert-butyl dicarbonate; ammonium bicarbonate; In 1,4-dioxane; for 18h; Boc-L-Serine (OMe) -OH (2.4g, 6. Ommols) was dissolved in dioxan (20mis) and to this was added pyridine (0.31 mis), di-tert-butyl dicarbonate (1.7g, 7. 8mmols) and ammonium hydrogen carbonate (0.62g, 7. 2mmols). After stirring for 18 hours the crude reaction mixture was concentrated in vacuo and re-suspended in ethyl acetate. This was washed with 1 M KHS04 and the organic layer dried over magnesium sulphate. After concentration the crude product was purified by flash chromatography to yield 0.55g of a clear oil. This was dissolved in ethylene glycol dimethyl ether (20mis) and to this was added Lawesson's reagent (2. 78mmols). After stirring at room temperature for 3 hours the reaction mixture was concentrated in vacuo and the residue purified by flash chromatography (silica gel, DCM) to give a yellow oil (2-Methoxy-1-thiocarbamoyl- ethyl)-carbamic acid tert-butyl ester (0.49g). The ester (0.25g, 1. 07mmols) was dissolved in ethanol (10mis) and 4- (2-Bromo-acetyl)- benzoic acid methyl ester (1. 18mmols, 0.30g) was added. The reaction was heated to 50°C for one hour. The crude product was purified by preparative HPLC (MeCN/H20) to yield 0.138g of a yellow solid. The Boc group was removed via treatment with 4M HCI/dioxan for one hour after which time the reaction mixture was concentrated in vacuo. The free amine (0.093g, 0. 265mmols) was then dimethylated. The crude HCI salt was dissolved in 5mis of methanol and buffered with 2. 5mis pH 5.5 Sodium acetate/acetic acid. Formaldehyde was added (0. 58mmols) and the reaction stirred for one hour. Sodium cyanoborohydride was then added (0. 58mmols, 0.036g) and the reaction stirred for a further thirty minutes. The reaction mixture was concentrated in vacuo and purified by preparative HPLC to yield 60mg of a yellow solid. Finally, the methyl ester was hydrolyse with 1 M LiOH (5mis) and dioxan (5mis) at room temperature for two hours. The reaction mixture was concentrated in vacuo and lyophilised from water to yield 62mg of the desired acid as the lithium salt. ESMS (M + H = 307.04)
With pyridine; di-tert-butyl dicarbonate; ammonium bicarbonate; In 1,4-dioxane; for 18h; Boc-L-Serine(OMe)-OH (2.4g, beta.Ommols) was dissolved in dioxan (2OmIs) and to this was added pyridine (0.31 mis), di-tert-butyl dicarbonate (1.7g, 7.8mmols) and ammonium hydrogen carbonate (0.62g, 7.2mmols). After stirring for 18 hours the crude reaction mixture was concentrated in vacuo and re-suspended in ethyl acetate. This was washed with 1 M KHSO4 and the organic layer dried over magnesium sulphate. After concentration the crude product was purified by flash chromatography to yield 0.55g of a clear oil. This was dissolved in ethylene glycol dimethyl ether (2OmIs) and to this was added Lawesson's reagent (2.78mmols). After stirring at room temperature for 3 hours the reaction mixture was concentrated in vacuo and the residue purified by flash chromatography (silica gel, DCM) to give a yellow oil (2-Methoxy-1-thiocarbamoyl- ethyl)-carbamic acid tert-butyl ester (0.49g). The ester (0.25g, 1.07mmols) was dissolved in ethanol (1OmIs) and 4-(2-Bromo-acetyl)- benzoic acid methyl ester (1.18mmols, 0.3Og) was added. The reaction was heated to 500C for one hour. The crude product was purified by preparative HPLC (MeCN/H2O) to yield 0.138g of a yellow solid. The Boc group was removed via treatment with 4M HCI/dioxan for one hour after which time the reaction mixture was concentrated in vacuo. The free amine (0.093g, 0.265mmols) was then dimethylated. The crude HCI salt was dissolved in 5mls of methanol and buffered with 2.5mls pH 5.5 Sodium acetate/acetic acid. Formaldehyde was added (0.58mmols) and the reaction stirred for one hour. Sodium cyanoborohydride was then added (0.58mmols, 0.036g) and the reaction stirred for a further thirty minutes. The reaction mixture was concentrated in vacuo and purified by preparative HPLC to yield 60mg of a yellow solid. Finally, the methyl ester was hydrolysed with 1 M LiOH (5mls) and dioxan (5mls) at room temperature for two hours. The reaction mixture was concentrated in vacuo and lyophilised from water to yield 62mg of the desired acid as the lithium salt. ESMS (M + H = 307.04)
 

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