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HRID 2093671作成日:2026年10月25日

Dichloromethane → (7R)-2-chloro-8-(1-cyclopropylethyl)-7-ethyl-5-methyl-7,8-dihydropteridin-6(5H)-one

https://huagongshe.com/reaction/2093671

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Cyclopropyl methyl ketoneHCID 13004—
反応物2,4-Dichloro-5-nitropyrimidineHCID 521266—
反応物methyl (2R)-2-aminobutanoate hydrochlorideHCID 13283516—
溶媒1,2-DichloroethaneHCID 11—
生成物(7R)-2-chloro-8-(1-cyclopropylethyl)-7-ethyl-5-methyl-7,8-dihydropteridin-6(5H)-oneHCID 58405334—

反応手順

Intermediate SS is prepared from compound I-SS via compound II-SS, III-SS and IV-SS similarly to the methods used in preparing compound III-J, Intermediate J-1, compound IV-J and Intermediate J as described above, with (R)-methyl 2-aminobutanoate hydrochloride used instead of (R)-methyl 2-aminobutanoate and with cyclopropylethanone instead of dihydro-2H-pyran-4(3H)-one in the first step, and with PE/dichloromethane instead of PE/1,2-dichloroethane as solvent in the coupling of 2,4-dichloro-5-nitropyrimidine with compound II-SS. Compound III-SS; LCMS: 343.1 m/z (M+H)+. Compound IV-SS; LCMS: 281.1 m/z (M+H)+. Intermediate SS. LCMS: 295 m/z (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08445503B2
出典データセットuspto-grants-2013_05
ORD IDord-32d933b31e7e4d52b7871c9ad1cf93ad
出典メモuspto-grants-2013_05