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ethyl 6-bromo-1H-pyrrolo[3,2-b]pyridine-3-carboxylate synthesis

3synthesis methods
(5-BroMo-3-nitropyridin-2-yl)acetic acid ethyl ester

1211540-74-7
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ethyl 6-bromo-1H-pyrrolo[3,2-b]pyridine-3-carboxylate

1615714-30-1
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-

Yield:-

Steps:

Multi-step reaction with 2 steps
1: N,N-dimethyl-formamide / 80 °C / Inert atmosphere
2: iron; acetic acid / 60 °C / Inert atmosphere

References:

Shirude, Pravin S.;Shandil, Radha K.;Manjunatha;Sadler, Claire;Panda, Manoranjan;Panduga, Vijender;Reddy, Jitendar;Saralaya, Ramanatha;Nanduri, Robert;Ambady, Anisha;Ravishankar, Sudha;Sambandamurthy, Vasan K.;Humnabadkar, Vaishali;Jena, Lalit K.;Suresh, Rudrapatna S.;Srivastava, Abhishek;Prabhakar;Whiteaker, James;McLaughlin, Robert E.;Sharma, Sreevalli;Cooper, Christopher B.;Mdluli, Khisi;Butler, Scott;Iyer, Pravin S.;Narayanan, Shridhar;Chatterji, Monalisa [Journal of Medicinal Chemistry,2014,vol. 57,# 13,p. 5728 - 5737]

911434-04-3 Synthesis
2-(5-BROMO-3-NITROPYRIDIN-2-YL)MALONIC ACID DIETHYL ESTER

911434-04-3
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ethyl 6-bromo-1H-pyrrolo[3,2-b]pyridine-3-carboxylate

1615714-30-1
21 suppliers
inquiry