戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 657007作成日:2026年10月25日

Triethylamine → phenylmethyl [((3R,4R)-4-hydroxy-1-{2-[7-(methyloxy)-2-oxo-1,5-naphthyridin-1(2H)-yl]ethyl}-3-pyrrolidinyl)methyl]carbamate

https://huagongshe.com/reaction/657007

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物(7-methoxy-2-oxo-1,5-naphthyridin-1(2H)-yl)acetaldehydeHCID 57815194—
反応物Phenylmethyl {[(3S,4R)-4-hydroxy-3-pyrrolidinyl]methyl}carbamateHCID 86616784—
溶媒Chloroform methanolHCID 21584188—
生成物phenylmethyl [((3R,4R)-4-hydroxy-1-{2-[7-(methyloxy)-2-oxo-1,5-naphthyridin-1(2H)-yl]ethyl}-3-pyrrolidinyl)methyl]carbamateHCID 8663533273%

反応手順

To a solution of [7-(methoxy)-2-oxo-1,5-naphthyridin-1(2H)-yl]acetaldehyde (as the methyl hemiacetal) (0.500 g, 2.29 mmol) in 1:1 (MeOH/CHCl3) (40 mL) were added phenylmethyl {[(3S,4R)-4-hydroxypyrrolidin-3-yl]methyl}carbamate (0.658 g, 2.29 mmol) and triethylamine (0.351 mL, 2.52 mmol). The resulting solution was stirred at ambient temperature for 1 h. Na(OAc)3BH (1.46 g, 6.87 mmol) was added and the solution stirred at rt for an additional 18 h. The reaction mixture was concentrated onto silica gel and chromatographed on a silica gel column [0-100% CHCl3/(90:10:1) CHCl3/MeOH/NH4OH)] to yield a colorless oil (0.760 g, 73%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08071592B2
出典データセットuspto-grants-2011_12
ORD IDord-06c0363007eb4083869ac5dd9aad6f0c
出典メモuspto-grants-2011_12