(6-Chloro-3-nitro(2-pyridyl))(methylsulfonyl)amine → {6-[(2-{[4-(2,4-Dichlorophenyl)-5-imidazolylpyrimidin-2-yl]amino}ethyl)amino]-3-nitro(2-pyridyl)}(methylsulfonyl)amine

참여 물질

역할	이름	HCID	투입량
반응물	(6-Chloro-3-nitro(2-pyridyl))(methylsulfonyl)amine	HCID 22142577	—
반응물	[4-(2,4-Dichlorophenyl)-5-imidazol-2-ylpyrimidin-2-yl]{2-[(6-methoxy-5-nitro(2-pyridyl)) amino]ethyl}amine	HCID 22142635	—
반응물	4-(2,4-Dichlorophenyl)-5-imidazolylpyrimidin-2-ylethylamine	HCID 54231773	—
생성물	{6-[(2-{[4-(2,4-Dichlorophenyl)-5-imidazolylpyrimidin-2-yl]amino}ethyl)amino]-3-nitro(2-pyridyl)}(methylsulfonyl)amine	HCID 22142954	—

반응 단계

{6-[(2-{[4-(2,4-dichlorophenyl)-5-imidazol-2-ylpyrimidin-2-yl]amino}ethyl)-amino]-3-nitro(2-pyridyl)}(methylsulfonyl)amine was prepared from [4-(2,4-dichlorophenyl)-5-imidazol-2-ylpyrimidin-2-ylethylamine and (6-chloro-3-nitro(2-pyridyl))(methylsulfonyl)amine in accordance with the procedure described above for the preparation of [4-(2,4-dichlorophenyl)-5-imidazol-2-ylpyrimidin-2-yl]{2-[(6-methoxy-5-nitro(2-pyridyl))amino]ethyl}amine.

출처 및 근거

DOI	10.6084/m9.figshare.5104873.v1
특허 번호	US07425557B2
출처 데이터셋	uspto-grants-2008_09
ORD ID	ord-c94a840f92f046628fffad8d7714adac
출처 메모	uspto-grants-2008_09