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Chemical Structure| 935668-23-8 Chemical Structure| 935668-23-8

Structure of 935668-23-8

Chemical Structure| 935668-23-8

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Product Details of [ 935668-23-8 ]

CAS No. :935668-23-8
Formula : C10H19NO3
M.W : 201.27
SMILES Code : O=C(N1[C@H](COC)CC1)OC(C)(C)C
MDL No. :MFCD30074763

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Application In Synthesis of [ 935668-23-8 ]

* 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 [ 935668-23-8 ]

[ 935668-23-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 161511-85-9 ]
  • [ 74-88-4 ]
  • [ 935668-23-8 ]
YieldReaction ConditionsOperation in experiment
93% With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20℃; for 1h; (S)-1-(tert-butoxycarbonyl)azetidine-2-methanol (5) (8.03 g, 42.9 mmol) was introduced into a 200-mL pear-shaped flask, and N,N-dimethylformamide (60 mL) was added to dissolve the compound. Methyl iodide (5.34 mL, 85.8 mmol) was added thereto. While stirring the content under ice cooling, sodium hydride (commercial product, purity 55%) (2.81 g, 64.3 mmol) was slowly added, and the mixture was stirred for one hour at room temperature. The reaction liquor was transferred to ice water, and the mixture was extracted with ethyl acetate (250 mLx2). The extract was dried over anhydrous sodium sulfate. After filtering the extract, the filtrate was concentrated under reduced pressure, and azeotropically boiled with toluene. The obtained concentrated residue was subjected to flash column chromatography (column size: 40M) manufactured by Biotage AB, and the fraction obtained from an elution with n-hexane:ethyl acetate (4:1, v/v) was concentrated under reduced pressure and dried, to obtain the title compound (8.05 g, 40.0 mmol, 93%) as a solid. NMR(CDCl3)δ:1.44(9H,s),2.11-2.27(2H,m),3.41-3.41(3H,m),3.55(1H,d,J=3.1Hz),3.62-3.69(1H,m),3.82(2H,t,J=8.1Hz),4.27-4.34(1H,m). MS(ESI)m/z:102(M++1-Boc).
Step 1: (S)-2-(Methoxymethyl)-1-azetidinecarboxylic acid tert-butyl ester; 60% Sodium hydride (240 mg) was suspended in N,N-dimethylformamide (12 ml), and the suspension was cooled on ice under a nitrogen atmosphere. The suspension was added dropwise with a solution of (2S)-2-(hydroxymethyl)-1-azetidinecarboxylic acid tert-butyl ester (936 mg) dissolved in N,N-dimethylformamide (6 ml), and then stirred for 20 minutes. Then, the reaction mixture was added with methyl iodide (0.40 ml), returned to room temperature, and stirred overnight. The reaction mixture was added with cooled saturated aqueous ammonium chloride, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel chromatography [developing solvent; ethyl acetate:n-hexane=1:4 (v/v)] to obtain the title compound (910 mg) as colorless oil. 1 H-NMR (400MHz, CDCl3) δ : 1.44 (9H, s), 2.11-2.27 (2H, m), 3.41 (3H, s), 3.54 (1H, dd, J=10, 3.2Hz), 3.65 (1H, dd, J=10, 5.4Hz), 3.81 (2H, dd, J=8.2, 6.9Hz), 4.27-4.33 (1H, m).
 

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