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HRID 655312作成日:2026年10月26日

Triphenylphosphine → 3-(4-Methylpiperazin-1-yl)propyl [3-(5-methyl-2-oxooxazolo-[4,5-b]pyridin-3-ylmethyl)phenyl]carbamate

https://huagongshe.com/reaction/655312

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Di-tert-butyl azodicarboxylateHCID 97268—
反応物5-Methyloxazolo[4,5-b]pyridin-2(3H)-oneHCID 10012075—
反応物3-(4-Methylpiperazin-1-yl)propyl (3-hydroxymethylphenyl)carbamateHCID 59564727—
溶媒DimethylformamideHCID 6228—
生成物3-(4-Methylpiperazin-1-yl)propyl [3-(5-methyl-2-oxooxazolo-[4,5-b]pyridin-3-ylmethyl)phenyl]carbamateHCID 59564715—

反応手順

98 mg (0.65 mmol) of 5-methyl-3H-oxazolo[4,5-b]pyridin-2-one, 200 mg (0.65 mmol) of 3-(4-methylpiperazin-1-yl)propyl (3-hydroxymethylphenyl)carbamate and 325 mg (0.98 mmol) of polymer-bound triphenylphosphine (3 mmol/g) are suspended in 5 ml of DMF, and the mixture is shaken for 30 min. 229 mg (0.98 mmol) of di-tert-butyl azodicarboxylate are subsequently added. The reaction mixture is shaken at room temperature. The reaction mixture is filtered and rinsed with THF, and the filtrate is evaporated. The residue is purified by column chromatography on silica gel.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08071593B2
出典データセットuspto-grants-2011_12
ORD IDord-829cde76b514485e9a04d8c2ab01967f
出典メモuspto-grants-2011_12