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HRID 518979作成日:2026年10月26日

Potassium Carbonate → 3-(7-Isopropenyl-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-ylamino)-azetidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/518979

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolaneHCID 10997426—
反応物3-(7-Bromo-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-ylamino)-azetidine-1-carboxylic acid tert-butyl esterHCID 86727293—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物3-(7-Isopropenyl-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-ylamino)-azetidine-1-carboxylic acid tert-butyl esterHCID 8672732984%

反応条件

温度80 °C

反応手順

A mixture of 3-(7-bromo-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-ylamino)-azetidine-1-carboxylic acid tert-butyl ester (Example 1, Step B, 1.5 g, 3.22 mmol), 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (1.62 g, 9.66 mmol), K2CO3 (1.33 g, 9.66 mmol) and [1,1′-Bis(diphenylphosphino)ferrocene]palladium(II) chloride (0.544 g, 0.64 mmol) in a mixture of 10% water in dioxane (35 mL) was heated at 80° C. for 2 h. The reaction mixture was cooled to ambient temperature and concentrated in vacuo. The residue was purified by column chromatography on silica gel (eluting with 20% EtOAc in petroleum ether) to give 3-(7-isopropenyl-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-ylamino)-azetidine-1-carboxylic acid tert-butyl ester (1.15 g, 84%) as a pale solid. LC/MS (Table 1, Method 2) Rt=1.202 min.; MS m/z: 428 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115151B2
出典データセットuspto-grants-2015_08
ORD IDord-0e7ff09fe45640ed92133ff55ebed7ab
出典メモuspto-grants-2015_08