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HRID 2147作成日:2026年10月23日

Water → 7-Demethoxy-7-oxorapamycin

https://huagongshe.com/ja/reaction/2147

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
反応物SirolimusHCID 5284616—
溶媒DichloromethaneHCID 6344—
生成物7-Demethoxy-7-oxorapamycinHCID 101680738—

反応手順

To a solution of rapamycin (5 mg, 0.055 mmol) in dichloromethane (0.1 mL) was added water (0.02 mL) followed by DDQ (2.4 mg, 0.011 mmol), and the resulting dark brown suspension was stirred at room temperature for 45 min. The mixture was filtered through celite and then partitioned between dichloromethane and brine; the organic extracts were dried over anhydrous magnesium sulfate and the resulting crude material was purified by prep TLC. The desired product was isolated as a colorless oil (1.2 mg). 1 H NMR (CDCl3, 400 MHz, 3:1 mixture of trans:cis amide rotamers; data for the trans-rotamer): -- 7.145 (d, J=10.4 Hz, 1H), 6.635 (dd, J=14.9, 10.6 Hz, 1H), 6.57-6.48 (m, 2H), 6.224 (dd, J=15.1, 10.6 Hz, 1H), 5.662 (dd, J=15.1, 8.6 Hz, 1H), 5.447 (d, J=11.2 Hz, 1H), 4.305 (br d, J=5.4 Hz, 1H), 3.983 (d, J=5.4 Hz, 1H), 3.385 (s, 3H), 3.346 (s, 3H),; MS (ESl+/NH4OAc) m/z 920 (M+Na+), 915 (M+NH4+), 898, 880; UV (MeOH) max 318 nm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728710
出典データセットuspto-grants-1998_03
ORD IDord-ff129fa8213d45ca8f4648e29b01c951
出典メモuspto-grants-1998_03