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ChemicalBook CAS DataBase List methyl 5-chloro-1H-indole-6-carboxylate

methyl 5-chloro-1H-indole-6-carboxylate synthesis

3synthesis methods
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Yield:1245643-61-1 52%

Reaction Conditions:

Stage #1: N,N-dimethylformamide diisopropyl acetal;methyl 2-chloro-4-methyl-5-nitrobenzoate in N,N-dimethyl-formamide at 130; for 3 h;
Stage #2: with acetic acid;zinc in water at 75 - 80;

References:

McCoull, William;Barton, Peter;Brown, Alastair J. H.;Bowker, Suzanne S.;Cameron, Jennifer;Clarke, David S.;Davies, Robert D. M.;Dossetter, Alexander G.;Ertan, Anne;Fenwick, Mark;Green, Clive;Holmes, Jane L.;Martin, Nathaniel;Masters, David;Moore, Jane E.;Newcombe, Nicholas J.;Newton, Claire;Pointon, Helen;Robb, Graeme R.;Sheldon, Christopher;Stokes, Stephen;Morgan, David [Journal of Medicinal Chemistry,2014,vol. 57,# 14,p. 6128 - 6140] Location in patent:supporting information

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