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HRID 595419作成日:2026年10月25日

Diisopropylethylamine → Methyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-hydroxypropanoate

https://huagongshe.com/reaction/595419

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Methyl DL-serinateHCID 416960—
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6-Chloro-4-(isopropylamino)nicotinic acidHCID 89689857—
溶媒DimethylformamideHCID 6228—
生成物Methyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-hydroxypropanoateHCID 89689704—

反応手順

To a stirred solution of 6-chloro-4-(isopropylamino)nicotinic acid (9) (1.3 g, 6.06 mmol) in DMF (25 mL), methyl 2-amino-3-hydroxypropanoate (12.11 mmol) and DIPEA (18.17 mmol) were added followed by the addition of HATU (30.3 mmol) to the reaction mixture and stirred at room temperature for 2 h. DMF was removed under reduced pressure. The residue obtained was diluted with EtOAC and washed with water and 10% NaHCO3 solution. The organic layer was collected, dried over Na2SO4, filtered and concentrated. The crude material obtained was purified by flash chromatography using silica gel and EtOAC: pet ether as eluent to afford the title compound, methyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-hydroxypropanoate. LC/MS: ZORBAX SB C18, 4.6×50 mm, 5 μm; Solvent A=10% MeOH: 90% H2O: 0.1% TFA; Solvent B=90% MeOH: 10% H2O: 0.1% TFA; gradient 0-100% B over 2 min (3 min run time); retention time: 1.312 min; LCMS (ES-API), m/z 316.0 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242975B2
出典データセットuspto-grants-2016_01
ORD IDord-c049cfffa0794d01b9b55a13482be0fc
出典メモuspto-grants-2016_01