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HRID 78564作成日:2026年10月26日

Sodium Carbonate → 3-Amino-6-(pyridin-3-yl)pyrazine-2-carboxylic acid

https://huagongshe.com/reaction/78564

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物TriphenylphosphineHCID 11776—
反応物Methyl 3-Amino-6-bromopyrazine-2-carboxylateHCID 227251—
反応物3-(Diethylboryl)pyridineHCID 642851—
触媒Palladium ChlorideHCID 24290—
溶媒1,2-DimethoxyethaneHCID 8071—
溶媒Ethyl AcetateHCID 8857—
生成物3-Amino-6-(pyridin-3-yl)pyrazine-2-carboxylic acidHCID 5947215483.4%

反応手順

A mixture of methyl 3-amino-6-bromo-pyrazine-2-carboxylate (8 g, 34.48 mmol), diethyl-(3-pyridyl)borane (6.084 g, 41.38 mmol), dichloropalladium; triphenylphosphane (1.210 g, 1.724 mmol) and disodium carbonate (51.70 mL of 2 M, 103.4 mmol) in DME (100 mL) were heated overnight at 80° C. The reaction mixture was cooled and EtOAc was added. The resultant precipitate was collected, treated with water and the resultant suspension heated and filtered hot. The solution was then allowed to cool and acidified with AcOH to approx pH 5. The precipitate was collected, washed with MeOH and dried to yield the product as a yellow powder (6.22 g, 83% Yield). 1H NMR (400.0 MHz, DMSO) d 7.49 (dd, J=4.8, 7.4 Hz, 1H), 7.60 (s, 2H), 8.44 (d, J=7.6 Hz, 1H), 8.57 (d, J=3.7 Hz, 1H), 8.97 (s, 1H) and 9.27 (s, 1H) ppm; MS (ES+) 217

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841308B2
出典データセットuspto-grants-2014_09
ORD IDord-90c9a609f1164fa2800eafbbc9caf6e9
出典メモuspto-grants-2014_09