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HRID 36134作成日:2026年10月25日

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

https://huagongshe.com/reaction/36134

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,6-TrimethylpyridineHCID 7953—
反応物(-)-CarnitineHCID 10917—
反応物TetrafluoroborateHCID 26255—
反応物Sodium periodateHCID 23667635—
反応物DichlorotetradecylphosphiteHCID 86748667—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物(R)-3-Carboxy-N,N,N-trimethyl-2-{[hydroxy(tetradecyloxy)phosphinyl]oxy}-1-propanaminium HydroxideHCID 86748666—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05412137
出典データセットuspto-grants-1995_05
ORD IDord-f07963c8584147a5b1e3af067d4981b6
出典メモuspto-grants-1995_05