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Chemical Structure| 24021-90-7 Chemical Structure| 24021-90-7

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Chemical Structure| 24021-90-7

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Product Details of [ 24021-90-7 ]

CAS No. :24021-90-7
Formula : C3H5N3O2
M.W : 115.09
SMILES Code : O=C1NN=C(CO)N1

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Application In Synthesis of [ 24021-90-7 ]

* 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.

  • Upstream synthesis route of [ 24021-90-7 ]
  • Downstream synthetic route of [ 24021-90-7 ]

[ 24021-90-7 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 24021-90-7 ]
  • [ 252742-72-6 ]
YieldReaction ConditionsOperation in experiment
90.7% With thionyl chloride In acetonitrile at 5 - 20℃; 5-Hydroxymethyl-2,4-dihydro[1,2,4]triazol-3-one (100 g, 869 mmol) and anhydrous acetonitrile (1 L) were added to a 5 L four-necked flask, and the system was cooled to 5 ° C. Then, SOCl2 (150 g, 1261 mmol) was slowly added to the system under stirring. After the addition, the system was slowly warmed up to room temperature, and the TLC plate was traced until the reaction was complete. Then the system was decompressed under high vacuum conditions (including unreacted SOCl2). EtOAc (1 L) and H2 (EtOAc) (EtOAc) (EtOAc) The organic phase was combined, and the organic phase was washed with brine (2×500 mL), and the solvent was evaporated from the organic phase. The residue was added to the mixture of n-heptane (1 L) for 2 hours, filtered, and dried at 50 ° C. 5-Chloromethyl-2,4-dihydro[1,2,4]triazol-3-one (solid, 105.2 g, yield 90.7percent).
87.4% With thionyl chloride In hexane; acetonitrile EXAMPLE 3 Preparation of 3-Chloromethyl-1,2,4-triazolin-5-one Thionyl chloride (19.9 g) was added, over five minutes, to a slurry of 3-hydroxymethyl-1,2,4-triazolin-5-one (17 g) in acetonitrile (170 ml) at 20° C. under a nitrogen atmosphere. The reaction mixture as aged at 20° C. for 18 hours. [Note: after 30 minutes all the starting material had dissolved. At 1 hour the product began to crystallise]. TLC analysis (SiO2; ethyl acetate/methanol(9/1); I2) indicated that the reaction was complete. Hexane(510 ml) was added in one portion, the reaction cooled in an ice bath for 1 hour and the product collected by filtration. The solid was washed with hexane(100 ml) and dried in vacuo. 3-Chloromethyl-1,2,4-triazolin-5-one(17.2 g) was obtained as a white solid in 87.4% yield. mp 197-199° C.; 1H NMR in d6 DMSO δ=4.43(2H, s, CH2), 11.48 (1H, s, NH) and 11.64(1H, s, NH)ppm and 13C NMR in d6 DMSO, δ=37.0(ClCH2), 144.4(CH2C=N) and 156.8 (NHCONH) ppm.
References: [1] Patent: CN109485613, 2019, A, . Location in patent: Paragraph 0022.
[2] Tetrahedron Letters, 2000, vol. 41, # 44, p. 8661 - 8664.
[3] Patent: US6297376, 2001, B1, .
[4] Patent: WO2017/106062, 2017, A1, . Location in patent: Page/Page column 65.
 

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