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Chemical Structure| 299397-03-8 Chemical Structure| 299397-03-8

Structure of 299397-03-8

Chemical Structure| 299397-03-8

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Product Details of [ 299397-03-8 ]

CAS No. :299397-03-8
Formula : C6H8N2O2
M.W : 140.14
SMILES Code : O=C1NC(C(O)C)=NC=C1

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Application In Synthesis of [ 299397-03-8 ]

* 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 [ 299397-03-8 ]

[ 299397-03-8 ] Synthesis Path-Downstream   1~1

  • 1
  • sodium (E)-3-ethoxy-3-oxoprop-1-en-1-olate [ No CAS ]
  • [ 89799-34-8 ]
  • [ 299397-03-8 ]
YieldReaction ConditionsOperation in experiment
232 g (38%) In diethyl ether; water; Step D: 2-(1-Hydroxy-ethyl)-3H-pyrimidin-4-one To a solution of ethyl 3-hydroxy-acrylate sodium salt (prepared according to the method of Preparation Twelve, Step C, 1301 g, 9.42 mol) in water (1.3 L) was added a solution of <strong>[89799-34-8]2-hydroxy-propionamidine hydrochloride</strong> (prepared according to the method of Preparation Twelve, Step B, 610 g, 4.9 mol) in water (1.3 L) at ambient temperature and stirred for 48 h. The solution was adjusted to pH 7.0 with acetic acid then continuously extracted with chloroform for 48 h. The extract was dried over sodium sulfate and filtered. The filtrate was concentrated to a solid, slurried in ethyl ether, filtered, and dried to give the title compound as a solid, 232 g (38%). mp: 121-124 C.; 1H NMR (DMSO-d6, 400 MHz) delta1.30 (d, 3H), 4.46 (q, 1H), 5.62 (br s, 1H), 6.13 (d, 1H), 7.80 (d, 1H).
In diethyl ether; water; Step D. 2-(1RS-Hydroxy-ethyl)-3H-pyrimidin-4-one To a solution of sodium 2-ethoxycarbonyl ethenolate (prepared according to the method of Preparation One, Step C, 1301 g, 9.42 mol) in water (1.3 L) was added an aqueous solution of <strong>[89799-34-8]2-hydroxy-propionamidine hydrochloride</strong> (prepared according to the method of Preparation One, Step B, 610 g, 4.9 mol) in water (1.3 L) at ambient temperature and stirred for 48 h. The solution was adjusted to pH 7.0 with acetic acid and then continuously extracted with chloroform for 48 h. The extract was dried over sodium sulfate and filtered. The filtrate was concentrated to a solid which was slurried in ethyl ether, filtered and the solid residue dried to give the title compound of Preparation One (232 g, 38%); mp: 121-124 C.; 1H NMR (DMSO-d6, 300 MHz)??1.45 (d, 1H), 4.42(q, 1H), 6.25-6.88 (bs, 1H).
 

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