戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 68448作成日:2026年10月24日

Diisopropylethylamine → HCID 178455419、化合物

https://huagongshe.com/ja/reaction/68448

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物4-Bromo-2-(2-bromo-ethyl)-benzenesulfonyl chlorideHCID 58016189—
反応物HCID 137328873HCID 137328873—
溶媒1,1-DichloroethaneHCID 6365—
生成物HCID 178455419HCID 17845541953.4%

反応手順

The mixture of 5-[3-Amino-2-(tert-butyl-dimethyl-silanyloxymethyl)-phenyl]-1-methyl-3-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-1H-pyridin-2-one (0.2 g, 0.36 mmol), 4-bromo-2-(2-bromo-ethyl)-benzenesulfonyl chloride (0.4 g, 1.08 mmol) and DIPEA (1 mL) in dichloroethane (10 mL) was microwaved at 120° C. for 30 min, then added 4-bromo-2-(2-bromo-ethyl)-benzenesulfonyl chloride (0.4 g, 1.08 mmol) and DIPEA (1 mL) and microwaved at 120° C. for 30 min. After repeating this process three times, the mixture was concentrated to afford a dark residue. Purification by silica gel chromatography (methylene chloride/acetone) afforded 0.15 g of 5-[3-(6-Bromo-1,1-dioxo-3,4-dihydro-1H-1lambda*6*-benzo[e][1,2]thiazin-2-yl)-2-(tert-butyl-dimethyl-silanyloxymethyl)-phenyl]-3-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-1H-pyridin-2-one as a pale solid MS (ESI) 796.2 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822457B2
出典データセットuspto-grants-2014_09
ORD IDord-477ae28da8294f06b142b4c898fd5dd7
出典メモuspto-grants-2014_09