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1H-Pyrrolo[3,2-b]pyridine-5-Methanol synthesis

2synthesis methods
1H-Pyrrolo[3,2-b]pyridine-5-carboxylic acid, ethyl ester

1261433-14-0
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1H-Pyrrolo[3,2-b]pyridine-5-Methanol

1346569-67-2
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Yield:1346569-67-2 75%

Reaction Conditions:

with lithium aluminium tetrahydride in tetrahydrofuran at 0; for 2 h;Inert atmosphere;

References:

Lingam, V. S. Prasadarao;Dahale, Dnyaneshwar H.;Rathi, Vijay E.;Shingote, Yogesh B.;Thakur, Rajni R.;Mindhe, Ajit S.;Kummari, Srinivas;Khairatkar-Joshi, Neelima;Bajpai, Malini;Shah, Daisy M.;Sapalya, Ratika S.;Gullapalli, Srinivas;Gupta, Praveen K.;Gudi, Girish S.;Jadhav, Satyawan B.;Pattem, Rambabu;Thomas, Abraham [Journal of Medicinal Chemistry,2015,vol. 58,# 20,p. 8292 - 8308] Location in patent:supporting information