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HRID 36134생성일: 2026년 10월 23일

2,4,6-Trimethylpyridine → (R)-3-Carboxy-N,N,N-trimethyl-2-{[hydroxy(tetradecyloxy)phosphinyl]oxy}-1-propanaminium Hydroxide

https://huagongshe.com/ko/reaction/36134

반응식

참여 물질

역할이름HCID투입량
반응물2,4,6-TrimethylpyridineHCID 7953—
반응물(-)-CarnitineHCID 10917—
반응물TetrafluoroborateHCID 26255—
반응물Sodium periodateHCID 23667635—
반응물DichlorotetradecylphosphiteHCID 86748667—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물(R)-3-Carboxy-N,N,N-trimethyl-2-{[hydroxy(tetradecyloxy)phosphinyl]oxy}-1-propanaminium HydroxideHCID 86748666—

반응 단계

To a solution of 16.4 gm of the tetrafluoroborate salt of L-carnitine and 26 gm of collidine in 263 ml of acetonitrile is added 29.4 gm of dichlorotetradecylphosphite. The reaction mixture is stirred at room temperature for 17 hours and then a solution of 21.1 gm of sodium metaperiodate in 48.7 ml of water is added. After stirring at room temperature for two hours, the reaction mixture is filtered through Celite and the filtrate is concentrated under vacuum. The residue is flash chromatographed on normal phase silica gel, initially with a 50/30/3 ratio of chloroform/methanol/concentrated ammonium hydroxide and then with a 50/30/10 ratio of the same solvent system to yield a product that is then flash chromatographed on LiChroprep RP-8 silica gel using gradients from water to acetonitrile and to methanol. The title compound is isolated as an amorphous solid, (m.p. ~190° C. [dec]; 31P NMR=0.324 ppm; [α]25 =-10.34 C=1.0 MeOH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05412137
출처 데이터셋uspto-grants-1995_05
ORD IDord-f07963c8584147a5b1e3af067d4981b6
출처 메모uspto-grants-1995_05