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HRID 453376作成日:2026年10月25日

Diisopropylamine → 2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamide

https://huagongshe.com/reaction/453376

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物Pyrimidin-5-amineHCID 344373—
反応物2-Methyl-5-nitrobenzoic acidHCID 519683—
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—
溶媒DimethylformamideHCID 6228—
生成物2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamideHCID 24823255—

反応手順

In a 2L round bottom flask with mechanical stirring was charged with 2-methyl-5-nitrobenzoic acid (20 g), HATU (38 g) and diisopropylamine (32 mL) in DMF (90 mL). This mixture was stirred for 30 min then pyrimidin-5-amine was added and the reaction was stirred for 18 hr. The LCMS showed complete conversion. DMF was removed under vacuum as much as possible then water was added and a solid precipitated out (use mechanical stirring). The tan solid was filtered and rinsed with water, then taken up in EtOAc, washed with brine, dried over MgSO4, filtered and concentrated down. The crude was taken up in EtOAc and the product 45 precipitated out. This was filtered and the filtrate was concentrated down and taken up in EtOAc/Hex. After standing overnight, more solids were filtered and were combined with the first crop. 2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamide 45 was obtained as a light yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08492404B2
出典データセットuspto-grants-2013_07
ORD IDord-8412d5d5f20e47908513066372e957b3
出典メモuspto-grants-2013_07