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HRID 268580作成日:2026年10月27日

Triethylamine → 3-O-Methylmycarose

https://huagongshe.com/reaction/268580

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物5-Bromovaleric acidHCID 16368—
反応物Pivaloyl chlorideHCID 62493—
反応物AzithromycinHCID 447043—
反応物Sodium BicarbonateHCID 516892—
溶媒DichloromethaneHCID 6344—
生成物3-O-MethylmycaroseHCID 5460588108.6%

反応手順

To a solution of 5-bromovaleric acid (1.282 g; 7.07 mmole) in dry CH2Cl2 (10 ml), 1 ml (7.23 mmole) of triethylamine, 868 mg (7.10 mmole) of 4-dimethyl-aminopyridine and 0.940 ml (7.63 mmole) of pivaloyl chloride were added. The solution was stirred for 2 hours at room temperature in a flow of argon and then a solution of azithromycin (2 g; 2.67 mmole) in 10 ml of dry CH2Cl2 was added. The reaction mixture was stirred for three days at room temperature. Subsequently, 60 ml of saturated NaHCO3 solution were added to the reaction mixture and the layers were separated. The aqueous layer was twice more extracted with 40 ml of CH2Cl2. The combined organic extracts were washed with a saturated NaCl solution, dried over K2CO3 and evaporated in a rotary evaporator. The obtained oily product was purified on a silica gel column (eluant: CH2Cl2:CH3OH:NH4OH=90:9:1.5). 511 mg of the pure product were obtained. MS(ES+): 912 (MH+)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07446097B2
出典データセットuspto-grants-2008_11
ORD IDord-1449190227d74d05b0f2c41f7f5975ce
出典メモuspto-grants-2008_11