5-CHLORO-1H-PYRROLO[3,2-B] PYRIDINE
5-CHLORO-1H-PYRROLO[3,2-B] PYRIDINE Basic information
- Product Name:
- 5-CHLORO-1H-PYRROLO[3,2-B] PYRIDINE
- Synonyms:
-
- 5-Chloro-4-azaindole,5-chloro-1H-pyrrolo[3,2-b]pyridine
- 1H-Pyrrolo[3,2-b]pyridine, 5-chloro-
- 5-CHLORO-1H-PYRROLO[3,2-B] PYRIDINE
- 5-Chloro-4-azaindole
- 5-cChloro-1H-pyrrolo[3,2-b]pyridine
- CAS:
- 65156-94-7
- MF:
- C7H5ClN2
- MW:
- 152.58
- Product Categories:
-
- Azaindoles
- Mol File:
- 65156-94-7.mol
5-CHLORO-1H-PYRROLO[3,2-B] PYRIDINE Chemical Properties
- Boiling point:
- 304.9±22.0 °C(Predicted)
- Density
- 1.425±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- form
- solid
- pka
- 13.75±0.40(Predicted)
- Appearance
- Light brown to yellow Solid
Safety Information
- Hazard Codes
- Xi
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 2933998090
5-CHLORO-1H-PYRROLO[3,2-B] PYRIDINE Usage And Synthesis
Uses
5-Chloro-1H-pyrrolo[3,2-B]pyridine can be used as an organic synthesis intermediate and a pharmaceutical intermediate, and is mainly used in laboratory research and development processes and chemical pharmaceutical production processes.
Synthesis
1420070-26-3
65156-94-7
General procedure for the synthesis of 5-chloro-1H-pyrrolo[3,2-B]pyridine from compound (CAS:1420070-26-3): 5-chloro-1H-pyrrolo[3,2-B]pyridine (1.01 g, 5.1 mmol) was dissolved in 20 mL of methanol. 1 mL of concentrated hydrochloric acid was added and the reaction mixture was stirred at 75 °C for 21 hours. After completion of the reaction, the solvent was removed by evaporation under reduced pressure and the residue was extracted by partitioning with saturated potassium carbonate solution and ethyl acetate. The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. Purification by fast column chromatography (eluent: ethyl acetate/hexane, 33:67, v/v) afforded 0.55 g (3.6 mmol, 71% yield) of the target product, 5-chloro-1H-pyrrolo[3,2-B]pyridine, as a light yellow solid with 95% purity.1H NMR (300 MHz, CDCl3 + DMSO-d6) δ 9.85 (br. s , 1H), 7.67 (d, J = 8.5 Hz, 1H), 7.47 (m, 1H), 7.10 (d, J = 8.5 Hz, 1H), 6.65 (m, 1H).HPLC/MS analysis (run time 9 min) showed a retention time of 4.27 min. Low resolution mass spectrometry (LRMS): m/z 153 ([M + H]+).
References
[1] Patent: EP2548876, 2013, A1. Location in patent: Paragraph 0283-0286
[2] Patent: WO2013/10880, 2013, A1. Location in patent: Page/Page column 83
5-CHLORO-1H-PYRROLO[3,2-B] PYRIDINESupplier
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 5108538618
- suger.wang@chemfuture.com
- Tel
- 86-027-67849912
- sales@chemwish.com
- Tel
- +86 (0) 571 85 58 67 18
- Tel
- 13817811078
- sales@jingyan-chemical.com
5-CHLORO-1H-PYRROLO[3,2-B] PYRIDINE(65156-94-7)Related Product Information
- ethyl 5-chloro-1H-pyrrolo[3,2-b]pyridine-2-carboxylate
- 6-Chloro-1,3-dihydro-2H-pyrrolo[3,2-c]pyridin-2-one
- 1H-Pyrrolo[2,3-b]pyridine-3-carbonitrile, 5-chloro-
- 5-CHLORO (1H)INDAZOLE
- 5-chloro-1,2,3,4-tetrahydro-1,6-naphthyridine
- 5-Chloro-6-azaindole-3-carboxaldehyde
- 5-Chloro-1H-pyrazolo[4,3-b]pyridine
- 5-Chloro-1,2,3,4-tetrahydroisoquinoline
- 5-CHLORO-1H-PYRAZOLO[3,4-C]PYRIDINE
- 5-Chloro-[1,2,4]triazolo[1,5-a]pyridine
- 5-CHLORO-3-HYDROXY (1H)INDAZOLE
- 5-CHLORO-1H-INDOL-3-METHYLAMINE
- 5-Chloro-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid
- 5-Chloro-1,3,4-thiadiazol-2-ylamine
- 6-Chloro-3H-1,2,3-triazolo[4,5-c]pyridine
- 5-CHLORO-1H-PYRROLO[2,3-C]PYRIDINE
- 5-Chloro-7-azaindole-3-carboxaldehyde
- 5-Chloro-7-azaindole-3-carboxylic acid Methyl ester