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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44752생성일: 2026년 10월 24일

Triethylamine → 4-[(3-Nitro[1,5]naphthyridin-4-ylamino)methyl]tetrahydropyran-4-ol

https://huagongshe.com/ko/reaction/44752

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Chloro-3-nitro-1,5-naphthyridineHCID 13122787—
반응물4-(Aminomethyl)oxan-4-olHCID 43608754—
용매DichloromethaneHCID 6344—
생성물4-[(3-Nitro[1,5]naphthyridin-4-ylamino)methyl]tetrahydropyran-4-olHCID 6691913793.7%

반응 단계

A solution of 4-chloro-3-nitro[1,5]naphthyridine (16.6 g, 79.0 mmol) in dichloromethane (250 mL) and triethylamine (14.3 mL, 102.7 mmol) was cooled to 4° C. A solution of 4-aminomethyltetrahydropyran-4-ol (11.4 g, 86.9 mmol) in dichloromethane (70 mL) was added dropwise over a period of 30 minutes. The reaction mixture was allowed to stir at ambient temperature over the weekend and then it was concentrated under reduced pressure. The residue was stirred with water (300 mL). The resulting solid was isolated by filtration, rinsed with water, and dried in a vacuum oven at 50° C. for 4 hours to provide 22.53 g of 4-[(3-nitro[1,5]naphthyridin-4-ylamino)methyl]tetrahydropyran-4-ol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541438B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-b13aac86498640cbb8957bf3bf6a0172
출처 메모uspto-grants-2013_09