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HRID 256675作成日:2026年10月27日

Carbon Disulfide → 9-[(4-fluorophenyl)methyl]-N-[1-(2-isothiocyanatoethyl)-4-piperidinyl]-9H-purin-8-amine

https://huagongshe.com/reaction/256675

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DisulfideHCID 6348—
反応物N-[1-(2-aminoethyl)-4-piperidinyl]-9-[(4-fluorophenyl)methyl]-9H-purin-8-amineHCID 19785318—
溶媒TetrahydrofuranHCID 8028—
生成物9-[(4-fluorophenyl)methyl]-N-[1-(2-isothiocyanatoethyl)-4-piperidinyl]-9H-purin-8-amineHCID 19785225—

反応手順

To a stirred and cooled (-10° C.) mixture of 5.6 parts of N,N'-methanetetraylbis[cyclohexanamine], 13.9 parts of carbon disulfide and 90 parts of tetrahydrofuran were added portionwise 10 parts of N-[1-(2-aminoethyl)-4-piperidinyl]-9-[(4-fluorophenyl)methyl]-9H-purin-8-amine. Upon completion, the temperature was allowed to rise to room temperature and the reaction mixture was evaporated, yielding 16 parts of 9-[(4-fluorophenyl)methyl]-N-[1-(2-isothiocyanatoethyl)-4-piperidinyl]-9H-purin-8-amine (compound 181).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05258380
出典データセットuspto-grants-1993_11
ORD IDord-1fec5526cad443858fa95e8c34d84e52
出典メモuspto-grants-1993_11