ChemicalBook--->CAS DataBase List--->129872-81-7

129872-81-7

129872-81-7 Structure

129872-81-7 Structure
IdentificationBack Directory
[Name]

2,4-Dichloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine
[CAS]

129872-81-7
[Synonyms]

2,4-Dichloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine
5H-Pyrrolo[3,2-d]pyrimidine,2,4-dichloro-5-methyl-
[Molecular Formula]

C7H5Cl2N3
[MDL Number]

MFCD12755925
[MOL File]

129872-81-7.mol
[Molecular Weight]

202.044
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,2-8°C
[Appearance]

Off-white to yellow Solid
Spectrum DetailBack Directory
[Spectrum Detail]

2,4-Dichloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine(129872-81-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,4-DICHLORO-5H-PYRROLO[3,2-D]PYRIMIDINE

63200-54-4

Iodomethane

74-88-4

2,4-Dichloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine

129872-81-7

1. 2,4-Dichloro-5H-pyrrolo[3,2-d]pyrimidine (600 mg, 3.19 mmol) and N,N-dimethylformamide (DMF, 5 mL) were added to a round-bottomed flask and stirred until completely dissolved. 2. Add iodomethane (544 mg, 3.83 mmol) and cesium carbonate (520 mg, 1.60 mmol) to the reaction system sequentially. 3. Stir the reaction for 24 hours at room temperature. 4. 4. After completion of the reaction, the reaction solution was poured into water and extracted with ethyl acetate. 5. The organic phases were combined, dried over anhydrous sodium sulfate, filtered and concentrated to give a yellow solid product. 6. Yield: 91%.

[References]

[1] Patent: CN107312006, 2017, A. Location in patent: Paragraph 0037-0039
[2] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 15, p. 3486 - 3492
[3] Patent: CN104177363, 2018, B. Location in patent: Paragraph 0247; 0250-0251
[4] Patent: WO2015/193168, A1. Location in patent: Page/Page column 59
[4] Patent: , 2015, . Location in patent: Page/Page column 59
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