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HRID 479271作成日:2026年10月25日

N-(6-Aminohexyl)-1-naphthalenesulfonamide → Naphthalene-1-sulfonic acid [6-(4-amino-quinazolin-2-ylamino)-hexyl]-amide

https://huagongshe.com/reaction/479271

反応式

関与物質

役割名称HCID仕込み量
反応物N-(6-Aminohexyl)-1-naphthalenesulfonamideHCID 4314—
反応物2-Chloroquinazolin-4-amineHCID 252879—
溶媒Isoamyl AlcoholHCID 31260—
生成物Naphthalene-1-sulfonic acid [6-(4-amino-quinazolin-2-ylamino)-hexyl]-amideHCID 9955360—

反応手順

A solution of naphthalene-1-sulfonic acid (6-aminohexyl)-amide (0.450 g) and 2-chloro-quinazolin-4-ylamine (see: U.S. Pat. No. 3,956,495) (0.264 g) in 20 ml of isopentylalcohol is heated up to 120° C. for 15 h. Concentration of the reaction mixture followed by chromatography on silica gel (B1) yields naphthalene-1-sulfonic acid [6-(4-amino-quinazolin-2-ylamino)-hexyl]-amide as a white powder, melting at 98-101° C. Rf (B1) 0.28, FAB-MS: (M+H)+=450. Analytical C26H29N5O2S+HCl+H2O+0.6 1,4 dioxane. m.p. 98-101° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06645774B1
出典データセットuspto-grants-2003_11
ORD IDord-758947999fcb431b8c7f3bb0eaccd5ed
出典メモuspto-grants-2003_11