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HRID 421764作成日:2026年10月27日

(8aR)-Octahydropyrrolo(1,2-a)pyrazine → Abt-639

https://huagongshe.com/reaction/421764

反応式

関与物質

役割名称HCID仕込み量
反応物(8aR)-Octahydropyrrolo(1,2-a)pyrazineHCID 7004239—
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-Chloro-4-fluoro-5-{[(2-fluorophenyl)amino]sulfonyl}benzoic acidHCID 66675867—
溶媒2-MethyltetrahydrofuranHCID 7301—
溶媒DimethylacetamideHCID 31374—
生成物Abt-639HCID 46851313—

反応手順

To 2-chloro-4-fluoro-5-{[(2-fluorophenyl)amino]sulfonyl}benzoic acid (0.9 g, 2.59 mmol) and 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate(V) (1.08 g, 2.85 mmol) in N,N-dimethylacetamide (6.4 mL) and 2-methyltetrahydrofuran (15 mL) was added (R)-octahydropyrrolo[1,2-a]pyrazine (0.46 g, 3.68 mmol) in 2-methyltetrahydrofuran (4 mL). The reaction was stirred at ambient temperature overnight and diluted with 2-methyltetrahydrofuran (15 mL). The organic solution was washed with 6% NaHCO3/6% NaCl (10 mL), and the aqueous layer was extracted with 2-methyltetrahydrofuran (15 mL). The combined organic layers were washed with 6% NaHCO3/6% NaCl (10 mL) and saturated NaCl (2×10 mL), and then concentrated. The residue was concentrated from ethanol (2×10 mL) to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101614B2
出典データセットuspto-grants-2012_01
ORD IDord-1fe2802fa0ba4453ae4fb4d27095d260
出典メモuspto-grants-2012_01