Identification | Back Directory | [Name]
5-Chloro-7-azaindole | [CAS]
866546-07-8 | [Synonyms]
5-Chloro-7-azaindol 5-CHLORO-7-AZAINDOLE 5-Chloro-7-azaindole,95% 3-Chloro-7H-pyrrolo[2,3-b]pyridine 5-CHLORO-1H-PYRROLO[2,3-B]PYRIDINE 1H-Pyrrolo[2,3-b]pyridine, 5-chloro- 5-Chloro-1H-pyrrolo[2,3-b]pyridine > 5-Chloro-7-azaindole ISO 9001:2015 REACH 5-Chloro-1H-pyrrolo[2,3-b]pyridine (CPP) 5-Chloro-1H-pyrrolo[2,3-b]pyridine, 97+% | [Molecular Formula]
C7H5ClN2 | [MDL Number]
MFCD06659676 | [MOL File]
866546-07-8.mol | [Molecular Weight]
152.58 |
Chemical Properties | Back Directory | [Melting point ]
161-162°C | [density ]
1.425±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
Powder | [pka]
12.97±0.40(Predicted) | [color ]
White to pale brown | [InChI]
InChI=1S/C7H5ClN2/c8-6-3-5-1-2-9-7(5)10-4-6/h1-4H,(H,9,10) | [InChIKey]
MFZQJIKENSPRSJ-UHFFFAOYSA-N | [SMILES]
C12NC=CC1=CC(Cl)=CN=2 |
Hazard Information | Back Directory | [Chemical Properties]
Yellow powder | [Uses]
5-Chloro-7-azaindole can be used as an organic synthesis intermediate and a pharmaceutical intermediate, and is mainly used in laboratory research and development processes and chemical and pharmaceutical production processes. | [Synthesis]
Step 3: Synthesis of 5-chloro-7-azaindole (Ib)
Under nitrogen protection, 25.0 g of 4-(2-amino-5-chloropyridin-3-yl)-2-methylbut-3-yn-2-ol, 120 mL of N-methylpyrrolidone, and 130 mL of water were added to a 500 mL double jacketed reactor. The mixture was heated to 75-80 °C (jacket temperature about 95 °C) and a vacuum of 350 mbar was applied at about 100 °C. Subsequently, 85 mL of 28% sodium hydroxide aqueous solution was slowly added dropwise over 30-45 minutes at 75-80°C. Upon completion of the dropwise addition, the dropping funnel was rinsed with 5 mL of water and the mixture was stirred at 78-81 °C overnight. The jacket temperature and vacuum need to be adjusted during stirring to maintain a steady distillate flow rate. Under typical laboratory conditions, 50 mL of the water/acetone mixture can be distilled in approximately 2 hours. Continuous water replenishment is required during the reaction to keep the reaction volume constant at about 270 mL. After the reaction is complete, the mixture is cooled to 50-55 °C and 60 mL of toluene is added. The two-phase mixture was stirred at 50-55 °C for 15-30 min, followed by standing for 15-30 min to separate the layers. After separating the aqueous layer, the aqueous layer was extracted with 3 x 50 mL of toluene at 50-55°C. The toluene layers were combined and washed with 5 x 40 mL of water at 50-55°C. The toluene layer was concentrated to dryness and the residue (17.3 g) was recrystallized with 90 mL of toluene to give 13.0 g (71% yield) of 5-chloro-7-azaindole (Ib) as light yellow crystals with an HPLC purity of 96.7% (% area). | [References]
[1] Patent: US2011/28511, 2011, A1. Location in patent: Page/Page column 14 |
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