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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44761생성일: 2026년 10월 24일

Ethyl orthopropionate → 1-[(4-Amino-2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)methyl]cyclopropanol

https://huagongshe.com/ko/reaction/44761

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl orthopropionateHCID 66995—
반응물1,1,1-TrimethoxybutaneHCID 123512—
반응물4-Chloro-3-nitroquinolineHCID 11275808—
반응물4-Chloro-3-nitronaphthyridineHCID 12543213—
반응물1-(Aminomethyl)cyclopropan-1-olHCID 12609623—
반응물1-(2-Aminoethyl)cyclopropanolHCID 55285781—
생성물1-[(4-Amino-2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)methyl]cyclopropanolHCID 57515495—

반응 단계

1-[(4-Amino-2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)methyl]cyclopropanol was prepared according to the general methods of Parts D through G of Example 84 using 1-(aminomethyl)cyclopropanol in lieu of 1-(2-aminoethyl)cyclopropanol in Part D, 4-chloro-3-nitronaphthyridine in lieu of 4-chloro-3-nitroquinoline in Part D, and trimethyl orthobutyrate in lieu of triethyl orthopropionate in Part F. The crude product was triturated with hot acetonitrile to provide a tan solid. Which was recrystallized from chloroform and hexanes and dried at 140° C. under vacuum to provide product as an off-white solid, mp 199-200° C. MS (ESI) m/z 298 (M+H)+; Anal. calcd for C16H19N5O: C, 64.63; H, 6.44; N, 23.55. Found: C, 64.32; H, 6.62; N, 23.67.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541438B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-63b69e7bbeda44119ec322bdaa6cb786
출처 메모uspto-grants-2013_09