戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 25517作成日:2026年10月24日

N-BOC-ethylenediamine → (2-{3-[5-(1H-Indol-2-yl)-2-methoxy-phenyl]-thioureido}-ethyl)-carbamic acid tert-butyl ester

https://huagongshe.com/ja/reaction/25517

反応式

関与物質

役割名称HCID仕込み量
反応物N-BOC-ethylenediamineHCID 187201—
反応物[5-(1H-indol-2-yl)-2-methoxy-phenyl]-isothiocyanateHCID 22568433—
溶媒Ethyl AcetateHCID 8857—
生成物(2-{3-[5-(1H-Indol-2-yl)-2-methoxy-phenyl]-thioureido}-ethyl)-carbamic acid tert-butyl esterHCID 10160475—

反応手順

The product from Example 26, Step A, [5-(1H-indol-2-yl)-2-methoxy-phenyl]-isothiocyanate, (0.272 g, 1.0 mmol) and mono-tert-butyloxycarbonyl ethylenediamine (0.156 g, 1.0 mmol) were heated briefly to 50° C. in ethyl acetate (20 mL). The reaction mixture was allowed to stand 1 hour at room temperature and was then concentrated. The residue was filtered through silica gel using hexanes/ethyl acetate as eluant The purest product-containing factions were combined, concentrated, and triturated with 3/1, hexanes/ethyl acetate, v/v, to give the product as an off-white solid (0.09 g), mp 159-160° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858739B2
出典データセットuspto-grants-2005_02
ORD IDord-95de29cb25ad480fbdd559d44282b7e6
出典メモuspto-grants-2005_02