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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2234318생성일: 2026년 10월 26일

4-Methyl-2-Pentanol → 4-[(2-cyclopentyl-4,4-diethyl-6-methyl-5-oxo-2,6,9,11-tetrazabicyclo[5.4.0]undeca-7,9,11-trien-10-yl)amino]-N-(2,2-dimethyl-3-pyrrolidin-1-yl-propyl)-3-methoxy-benzamide

https://huagongshe.com/reaction/2234318

반응식

참여 물질

역할이름HCID투입량
반응물4-Methyl-2-PentanolHCID 7910—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물4-amino-N-(2,2-dimethyl-3-pyrrolidin-1-yl-propyl)-3-methoxy-benzamideHCID 68685881—
반응물10-Chloro-2-cyclopentyl-4,4-diethyl-6-methyl-2,6,9,11-tetrazabicyclo[5.4.0]undeca-7,9,11-trien-5-oneHCID 86617563—
용매MethanolHCID 887—
생성물4-[(2-cyclopentyl-4,4-diethyl-6-methyl-5-oxo-2,6,9,11-tetrazabicyclo[5.4.0]undeca-7,9,11-trien-10-yl)amino]-N-(2,2-dimethyl-3-pyrrolidin-1-yl-propyl)-3-methoxy-benzamideHCID 6868492327.5%

반응 조건

온도120 °C

반응 단계

10-chloro-2-cyclopentyl-4,4-diethyl-6-methyl-2,6,9,11-tetrazabicyclo[5.4.0]undeca-7,9,11-trien-5-one (Intermediate 250; 111 mg, 0.33 mmol), p-toluenesulphonic acid monohydrate (155 mg, 0.81 mmol) and 4-amino-N-(2,2-dimethyl-3-pyrrolidin-1-yl-propyl)-3-methoxy-benzamide (Intermediate 206; 100 mg, 0.33 mmol) were added to 4-methyl-2-pentanol (7 mL). The reaction was heated at 120° C. over the weekend. The sample was transferred to an SCX cartridge (10 g) pre-wet with methanol, then washed with methanol and eluted with methanolic ammonia. Product containing fractions were combined and evaporated and the resultant material purified by base modified reverse phase preparative HPLC to yield the title compound as a white solid (55 mg, 27%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07709471B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-60b4843b9356418ca573b23f27335ab6
출처 메모uspto-grants-2010_05