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HRID 246749作成日:2026年10月26日

Ethylamine → 2-Bromo-N-isopropyl-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide

https://huagongshe.com/reaction/246749

反応式

関与物質

役割名称HCID仕込み量
反応物EthylamineHCID 6341—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物2-bromo-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acidHCID 86677897—
溶媒TetrahydrofuranHCID 8028—
生成物2-Bromo-N-isopropyl-5H-pyrrolo[2,3-b]pyrazine-7-carboxamideHCID 8667801061.7%

反応手順

A mixture of 2-bromo-5H-pyrrolo[3,2-b]pyrazine-7-carboxylic acid (250 mg, 1.03 mmol), ethanamine (0.2 mL 2.2 mmol) and HATU (456 mg, 1.2 mmol) in 20 mL of dry THF was stirred for 4 hours at room temperature. The reaction mixture was evaporated to dryness, the residue was suspended in 20 mL of 0.5 N HCl, product extracted with ethyl acetate (3×50 mL), organics combined dried with sodium sulfate, filtered and concentrated. Residue purified by column chromatography (silica gel, 200-300 mesh, eluting with ethyl acetate/petroleum ether 2:1) to give 2-bromo-N-isopropyl-5H-pyrrolo[3,2-b]pyrazine-7-carboxamide (180 mg, 43%). LCMS: (M+H)+=269/271; 1H NMR (300 MHz, CD3OD): δ 12.95 (s, 1H), 8.50 (s, 1H), 8.43 (s, 1H), 7.77-7.72 (m, 1H), 3.42-3.36 (m, 2H), 1.25-1.12 (m, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658646B2
出典データセットuspto-grants-2014_02
ORD IDord-7d639397bdcd43269bbe02c77454d465
出典メモuspto-grants-2014_02