Identification | Back Directory | [Name]
ASISCHEM A03574 | [CAS]
110099-94-0 | [Synonyms]
ASISCHEM A03574 ASISCHEM A03574 ISO 9001:2015 REACH 2-(Methylthio)pyrimidine-5-carboxylicaci 2-(METHYLTHIO)PYRIMIDINE-5-CARBOXYLIC ACID 2-(Methylthio)-5-pyrimidinecarboxylic acid 5-Pyrimidinecarboxylic acid, 2-(methylthio)- 2-(methylthio)pyrimidine-5-carboxylic acid(SALTDATA: FREE) | [Molecular Formula]
C6H6N2O2S | [MDL Number]
MFCD07394096 | [MOL File]
110099-94-0.mol | [Molecular Weight]
170.19 |
Chemical Properties | Back Directory | [Melting point ]
264-266 °C | [Boiling point ]
378.4±15.0 °C(Predicted) | [density ]
1.45 | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [pka]
2.82±0.10(Predicted) | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Uses]
2-(Methylthio)-5-pyrimidinecarboxylic Acid was useful for studying antimycotic activity of methyl 2,4-disubstituted 5-pyrimidinecarboxylates, 2,?4-?disubstituted 5-?pyrimidinecarboxylic acids and 2,?4-?disubstituted pyrimidines. | [Synthesis]
General procedure for the synthesis of 2-(methylthio)pyrimidine-5-carboxylic acid from ethyl 2-(methylthio)pyrimidine-5-carboxylate: Synthesis Example 29; Synthesis of Compound 167; Ethyl 2-(methylthio)-5-pyrimidinecarboxylate (1 g, 5 mmol) was dissolved in methanol (15 mL). 1N sodium hydroxide solution (6 mL) was added and the reaction mixture was stirred for 1 hour. Methanol was removed by rotary evaporator and concentrated. Hydrochloric acid (500 μL) was added and the resulting precipitate was filtered, washed with water and dried under vacuum to give 811 mg (95% yield) of the target product. The resulting pyrimidine carboxylic acid was coupled with 4-fluoroaniline using EEDQ (as described in Synthesis Example 1) to give 911 mg (73% yield) of pyrimidine formamide intermediate. The thiomethyl ether portion of pyrimidine formamide (800 mg, 3.1 mmol) was oxidized with m-chloroperoxybenzoic acid (530 mg, 3.1 mmol) in acetonitrile (150 mL) for 1 hr at room temperature, and the resulting precipitate was filtered and dried under vacuum to give 300 mg (35% yield) of the oxidized product. The crude product (300 mg) was dissolved in anhydrous N,N-dimethylformamide (20 mL) and sodium sulfide (124 mg, 2 mmol) was added. The reaction mixture was gently refluxed for 2 h. Ethyl acetate (100 mL) was subsequently added and the organic layer was washed with water. The organic solvent was removed by rotary evaporator and the 6-mercapto-pyrimidinecarboxamide intermediate was purified by preparative HPLC to give 18 mg of product. Finally, alkylation of 6-mercapto-pyrimidinecarboxamide with 2-bromomethyl-phenylboronic acid using Method B afforded 10 mg (36% yield) of compound 163 as a white solid.ESI-MS m/z = 384.0 [M + H]+. | [References]
[1] Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, 1986, vol. 40, # 9, p. 764 - 767 [2] Patent: US2010/210593, 2010, A1. Location in patent: Page/Page column 50 [3] Patent: EP2942346, 2015, A1. Location in patent: Paragraph 0191 [4] Patent: WO2017/176812, 2017, A1. Location in patent: Paragraph 0389 [5] Journal of Chemical Research, 2007, # 8, p. 490 - 493 |
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