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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 554076생성일: 2026년 10월 25일

2,4-Dichlorobenzylamine → Gsk1370319A

https://huagongshe.com/reaction/554076

반응식

참여 물질

역할이름HCID투입량
반응물2,4-DichlorobenzylamineHCID 1485—
반응물DiisopropylamineHCID 7912—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물(2S)-1-methyl-5-oxopyrrolidine-2-carboxylic acidHCID 18649403—
용매Dimethyl SulfoxideHCID 679—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물Gsk1370319AHCID 6746178870.6%

반응 조건

온도20 °C

반응 단계

1-Methyl-5-oxo-proline (0.057 g, 0.4 mmol, prepared as described below) was dissolved in anhydrous dichloromethane (6 ml) and to this was added 1-hydroxybenzotriazole (0.060 g, 0.4 mmol), [(2,4-dichloro-phenyl)methyl]amine (0.055 ml, 0.4 mmol), diisopropylamine (0.140 ml, 0.8 mmol) and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.152 g, 0.4 mmol). The mixture was stirred at room temperature (20° C.) under argon for 3 hrs and then overnight. The mixture was diluted with more dichloromethane (25 ml) and washed sequentially with 2M aqueous hydrogen chloride (20 ml), saturated aqueous sodium hydrogen carbonate (20 ml), 10% aqueous sodium carbonate (20 ml) and brine (20 ml). The organic layer was filtered through a hydrophobic frit and then evaporated to give the crude product. The crude material was dissolved in a mixture of dimethylsulphoxide (0.9 ml) and acetonitrile (0.9 ml) and then purified by mass-directed automated HPLC to give pure N-[(2,4-dichlorophenyl)methyl]-1-methyl-5-oxo-prolinamide (0.085 g) as a white solid. LC/MS [M+H]+=301, retention time=2.16 minutes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08048907B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-265cbaacd23e4bdc9fd0dcecbe7c6695
출처 메모uspto-grants-2011_11