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HRID 38518作成日:2026年10月26日

Hydrochloric Acid → 3-(5,6,7,8-Tetrahydropyrido[4',3':4,5]thieno[2,3-d]pyrimidin-4-ylamino)phenol

https://huagongshe.com/reaction/38518

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物3-AminophenolHCID 11568—
反応物1,4-DioxaneHCID 31275—
反応物tert-Butyl 4-chloro-5,6-dihydropyrido(4',3':4,5)thieno(2,3-d)pyrimidine-7(8H)-carboxylateHCID 49788563—
触媒1,4-DioxaneHCID 31275—
溶媒IsopropanolHCID 3776—
生成物3-(5,6,7,8-Tetrahydropyrido[4',3':4,5]thieno[2,3-d]pyrimidin-4-ylamino)phenolHCID 58116796132.1%

反応条件

温度80 °C

反応手順

tert-Butyl 4-chloro-5,8-dihydropyrido[4′,3′:4,5]thieno[2,3-d]pyrimidine-7(6H)-carboxylate from Example 11A (1.00 g, 3.07 mmol) was dissolved in 2-propanol (10 mL). 3-Aminophenol (352 mg, 3.22 mmol) and a 4 M solution of gaseous hydrogen chloride in dioxane (38 μL, 0.15 mmol) were added, and the mixture was heated to 80° C. for 20 h. Subsequently, further 4 M hydrogen chloride in dioxane (1.54 mL, 6.14 mmol) was added, and the mixture was heated for additional 3 h. The precipitate was collected by suction filtration to yield 1.21 g of the title compound as hydrochloride salt. An analytical amount was dissolved in 1 M aqueous sodium hydroxide solution which was then concentrated in vacuo. The precipitate was collected by suction filtration and dried to yield the product as free base.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524722B2
出典データセットuspto-grants-2013_09
ORD IDord-0151bcdc251a4abcaaf0212cc6228d57
出典メモuspto-grants-2013_09