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ChemicalBook CAS DataBase List ethyl 5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylate
800401-67-6

ethyl 5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylate synthesis

4synthesis methods
800401-66-5 Synthesis
ETHYL 3-(2-CHLORO-5-NITROPYRIDIN-4-YL)-2-OXOPROPANOATE

800401-66-5
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Yield:800401-67-6 84%

Reaction Conditions:

with iron;ammonium chloride in tetrahydrofuran;ethanol at 20; for 2 h;Reflux;

Steps:

1a.2
Step 2: synthesis of ethyl 5-chloro-lH-pyrrolo[2,3-c]pyridine-2-carboxylate 10-bTo a solution of ethyl 3-(2-chloro-5-nitropyridin-4-yl)-2-oxopropanoate 10-a (2.726 g, 10 mmoles) in THF (80 mL) and EtOH (30 mL) was added a saturated solution of ammonium chloride (50 mL). Then, iron (2.747 g, 4.9 eq) was added portionwise under vigorous stirring to the mixture at room temperature, which was subsequently heated at reflux for 2h. The mixture was cooled down to RT, filtered over dicalite and washed with warm THF/ethanol 1/1. The filtrate was evaporated and the residue was stirred and refluxed in 100 mL water. The resulting precipitate was filtered off hot, washed twice with warm water and then dried in vacuo to provide 1.9 g (84% yield) of the targeted compound 10-b. m/z = 225 (M+H)+; 1H MR (400 MHz, OMSO-d6) ppm 1.36 (t, J = 6.8 Hz, 3H), 4.39 (q, J = 6.7 Hz, 2H), 7.15 (s, lH), 7.76 (s, lH), 8.64 (s, lH), 12.59 (br s,lH).

References:

JANSSEN R&D IRELAND;COOYMANS, Ludwig Paul;DEMIN, Samu?l Dominique;HU, Lili;JONCKERS, Tim Hugo Maria;RABOISSON, Pierre Jean-Marie Bernard;TAHRI, Abdellah;VENDEVILLE, Sandrine Marie Helene WO2012/80450, 2012, A1 Location in patent:Page/Page column 24

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