Azane;hydrate → 2-ethyl-1H-pyrrolo[2,3-c]pyridin-5-amine
Reaction equation
[CH2:1]([C:3]1[NH:12][C:6]2=[CH:7][N:8]=[C:9](Cl)[CH:10]=[C:5]2[CH:4]=1)[CH3:2].[NH3:13].O>CCO>[CH2:1]([C:3]1[NH:12][C:6]2=[CH:7][N:8]=[C:9]([NH2:13])[CH:10]=[C:5]2[CH:4]=1)[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 200 °C
Procedure
A suspension of 2-ethyl-5-chloro-1H-pyrrolo[2,3-c]pyridine (1.3 g, 7.19 mmol) in EtOH (20 mL), CuSO4.5H2O (179 mg, 0.72 mmol) and NH3.H2O (60 ml) was added into an autoclave (100 mL). The reaction was stirred at 200° C. and 2 MPa for 10 h. The reaction was cooled to 25° C. and was quenched with water and extracted with ethyl acetate (100 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (petroleum ether/ethyl acetate, 10/1) to give 2-ethyl-1H-pyrrolo[2,3-c]pyridin-5-amine (190 mg, 16%).
Workup
- additionwas added into an autoclave (100 mL)
- temperatureThe reaction was cooled to 25° C.
- customwas quenched with water
- extractionextracted with ethyl acetate (100 mL×3)
- dry with materialThe combined organic layers were dried over anhydrous Na2SO4
- customevaporated under reduced pressure
- customThe residue was purified by column chromatography on silica gel (petroleum ether/ethyl acetate, 10/1)
Sources & evidence
- ORD record
- ord-49a857d4b2434eadb2e7a4a8f70c74a8
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09102672B2
Reaction notes
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