戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1038961作成日:2026年10月27日

Methanol → 4-(6,7-Dimethoxy-9H-1,3,9-triaza-fluoren-4-yl)-piperazine-1-carbothioic acid(benzo[1,3]dioxol-5-ylmethyl)-amide

https://huagongshe.com/reaction/1038961

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物PyridineHCID 1049—
反応物6,7-dimethoxy-4-piperazino-9H-pyrimido[4,5-b]indoleHCID 14293784—
反応物N-Benzo[1,3]dioxol-5-ylmethyl-thioformamide chlorideHCID 86601006—
溶媒DichloromethaneHCID 6344—
生成物4-(6,7-Dimethoxy-9H-1,3,9-triaza-fluoren-4-yl)-piperazine-1-carbothioic acid(benzo[1,3]dioxol-5-ylmethyl)-amideHCID 11237489—

反応手順

To a solution of 6,7-dimethoxy-4-piperazino-9H-pyrimido[4,5-b]indole (200 mg, 0.64 mmol) and pyridine (0.5 mL, 6.4 mmol) in dichloromethane (20 mL) was added the solution of product 1c in dichloromethane (20 mL) and the mixture was stirred overnight. Methanol was added to quench excess thiophosgene, and the residue after removal of solvent was purified by silica gel column chromatography eluting with 5% methanol/dichloromethane and further recrystallized from dichloromethane/hexane to give 130 mg (40%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08552018B2
出典データセットuspto-grants-2013_10
ORD IDord-e4c8773b870a4fc5b7790b7b3aa24577
出典メモuspto-grants-2013_10