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2-Chloro-5H-pyrrolo[3,2-d]pyrimidine

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2-Chloro-5H-pyrrolo[3,2-d]pyrimidine Basic information
Product Name:2-Chloro-5H-pyrrolo[3,2-d]pyrimidine
Synonyms:2-Chloro-5H-pyrrolo[3,2-d...;2-chloro-5H-pyrrolo[3;5H-Pyrrolo[3,2-d]pyriMidine, 2-chloro-;2-chloro-1H-pyrrolo[3,2-d]pyrimidine;2-chloro-5H-pyrrolo[3,3-d]pyrimidine;2-chloro-5H-pyrrolo[3,2-d]pyrimidine, 95%min;2-Chloro-5H-pyrrolo[3,2-d]pyrimidine
CAS:1119280-66-8
MF:C6H4ClN3
MW:153.57
EINECS:
Product Categories:Heterocycle-Pyrimidine series
Mol File:1119280-66-8.mol
2-Chloro-5H-pyrrolo[3,2-d]pyrimidine Structure
2-Chloro-5H-pyrrolo[3,2-d]pyrimidine Chemical Properties
Melting point >230 °C
density 1.531±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka12.25±0.40(Predicted)
AppearanceOff-white to light yellow Solid
Safety Information
MSDS Information
2-Chloro-5H-pyrrolo[3,2-d]pyrimidine Usage And Synthesis
Synthesis
2,4-DICHLORO-5H-PYRROLO[3,2-D]PYRIMIDINE

63200-54-4

2-CHLORO-5H-PYRROLO[3,2-D]PYRIMIDINE

1119280-66-8

2,4-Dichloro-5H-pyrrolo[3,2-d]pyrimidine (134 mg, 0.71 mmol) was used as a feedstock and mixed with NaHCO3 (66 mg, 0.78 mmol) and 10% Pd/C (1.52 mg) in ethanol (4 mL). The reaction mixture was stirred at room temperature for 2.5 h under hydrogen (3 psi) atmosphere. Upon completion of the reaction, the mixture was filtered through a diatomaceous earth plug and the filtrate was evaporated. The residue was purified by fast chromatography to afford 2-chloro-5H-pyrrolo[3,2-d]pyrimidine (90 mg, 88% yield).LC/MS analytical conditions: gradient elution of 20-100% CH3CN with 0.05% HCOOH (aqueous) over 5 min, retention time of 1.58 min, and a molecular ion peak of [M+H]+ of 154 detected.

References[1] Patent: US2016/46597, 2016, A1. Location in patent: Paragraph 0220
[2] Journal of Medicinal Chemistry, 2018,
[3] Patent: CN105859726, 2016, A. Location in patent: Paragraph 0042; 0043; 0044
Tag:2-Chloro-5H-pyrrolo[3,2-d]pyrimidine(1119280-66-8) Related Product Information
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