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HRID 80936作成日:2026年10月23日

Hydrochloric Acid → 2-[4-(4-Isopropyl-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-5'-yl)phenoxy]-N,N-dimethylacetamide, dihydrochloride

https://huagongshe.com/ja/reaction/80936

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Sodium hydrideHCID 24758—
反応物2-chloro-N,N-dimethylacetamideHCID 75886—
反応物HCID 136099407HCID 136099407—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物2-[4-(4-Isopropyl-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl-5'-yl)phenoxy]-N,N-dimethylacetamide, dihydrochlorideHCID 13173078641%

反応手順

4-(4-Isopropyl-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl-5′-yl)phenol (0.15 g, 0.404 mmol) was dissolved in DMF (4 mL) in a 5 mL microwave vial. NaH (0.039 g, 1.62 mmol) was added slowly and the mixture was stirred at rt for 30 min. Chloro-N,N-dimethylacetamide (0.147 g, 1.21 mmol) was added and the reaction mixture was heated for 2.5 h at 130° C. in a microwave oven. The reaction mixture was evaporated in vacuo and the residue was redissolved in a mixture of DCM and water. The phases were separated and the aqueous phase was extracted with DCM (2×25 mL). The combined organic extracts were evaporated, redissolved in MeOH and purified by preparative HPLC Method B. This afforded an oil which was treated with HCl in diethyl ether to give a solid material. Recrystallization from acetone and MeOH afforded 75 mg (41%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846677B2
出典データセットuspto-grants-2014_09
ORD IDord-e49e647437524d0ebcef3596546110ac
出典メモuspto-grants-2014_09