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Chemical Structure| 700871-81-4 Chemical Structure| 700871-81-4

Structure of 700871-81-4

Chemical Structure| 700871-81-4

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Product Details of [ 700871-81-4 ]

CAS No. :700871-81-4
Formula : C15H19N3O3
M.W : 289.33
SMILES Code : O=C(OCC)C/C(C1=NC(C)=CC=C1)=N/N2C(CCC2)=O

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Application In Synthesis of [ 700871-81-4 ]

* 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 [ 700871-81-4 ]

[ 700871-81-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 150401-96-0 ]
  • [ 20386-22-5 ]
  • [ 700871-81-4 ]
YieldReaction ConditionsOperation in experiment
With pyridine; at 20℃; for 20h; B. Preparation of 3-[6-Methyl-(pyridin-2-yl)]-3-(2-oxo-pyrrolidin-l-ylimino)-propionic acid ethyl ester; EPO <DP n="16"/> Add l-aminopyrrolidin-2-one hydrochloride (Zubek, A. Z. Chem. 1969, 9(2), 58; 99.4 g, 0.73 mol) to a 3 L flask equipped with mechanical stirrer and nitrogen inlet. Add 3-[6-methyl-(pyridin-2-yl)]-3-oxo-propionic acid ethyl ester (Preparation 1, Part A; 154 g, 0.66 mol), and pyridine (280 mL). Stir the reaction mixture at room temperature for 20 h. Dilute the mixture with water (200 mL) and extract with toluene (2 x 250 mL).Combine the organic layers, filter, and concentrate in vacuo to yield the subtitled product (201 g) as a dark oil. MS (ES) m/z = 290 (M+H).
With pyridine; at 20℃; for 20h; Add L-AMINOPYRROLIDIN-2-ONE hydrochloride (Zubek, A. Z Chem. 1969, 9 (2), 58; 99.4 g, 0.73 mol) to a 3L flask equipped with mechanical stirrer and nitrogen inlet. Add 3- (6-methyl-pyridin-2-yl)-3-oxo-propionic acid ethyl ester (Preparation 1, Part A; 154 g, 0.66 mol), then pyridine (280 mL). Stir the reaction mixture at room temperature for 20 h. Dilute the mixture with water (200 mL) and extract with toluene (2 x 250 mL). Combine the organic layers, filter, and concentrate in vacuo to yield the subtitled product (201 g) as a dark oil. MS ES+ m/e 290 (M+1).
In pyridine; at 20℃; for 20h; Add l-aminopyrrolidin-2-one hydrochloride (Zubek, A. Z Chem. 1969, 9 (2), 58 ; 99.4 g, 0.73 mol) to a 3 L flask equipped with mechanical stirrer and nitrogen inlet. Add 3- [6-methyl- (pyridin-2-yl)]-3-oxo-propionic acid ethyl ester (154 g, 0.66 mol), and pyridine (280 mL). Stir the reaction mixture at room temperature for 20 h. Dilute the mixture with water (200 mL) and extract with toluene (2 x 250 mL). Combine the organic layers, filter, and concentrate in vacuo to yield the subtitled product (201 g) as a dark oil. MS ES+ m/e 290 (M+1).
 

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