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HRID 639288作成日:2026年10月27日

Benzo-1,3-dioxole-5-methylamine → N-(1,3-Benzodioxol-5-ylmethyl)-10-{[(4-bromophenyl)thio]acetyl}-10,11-dihydro-5H-pyrrolo[2,1-C][1,4]benzodiazepine-3-carboxamide

https://huagongshe.com/reaction/639288

反応式

関与物質

役割名称HCID仕込み量
反応物Benzo-1,3-dioxole-5-methylamineHCID 75799—
反応物2,2,2-trichloro-1-[10-{[(4-bromophenyl)thio]acetyl}-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-3-yl]-ethanoneHCID 16039367—
生成物N-(1,3-Benzodioxol-5-ylmethyl)-10-{[(4-bromophenyl)thio]acetyl}-10,11-dihydro-5H-pyrrolo[2,1-C][1,4]benzodiazepine-3-carboxamideHCID 16039440—

反応手順

The title compound was synthesized in the manner of Example 81 from 2,2,2-trichloro-1-[10-{[(4-bromophenyl)thio]acetyl}-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-3-yl]-ethanone of Example 80 and C-benzo[1,3]dioxol-5-yl-methylamine, m.p. 154-155° C. MS [(+)ESI, m/z]: 590 [M+H]+ Anal. Calcd for C29H24BrN3O4S: C, 58.99; H, 4.10; N, 7.12. Found: C, 58.96; H, 4.26; N, 7.03.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07691848B2
出典データセットuspto-grants-2010_04
ORD IDord-1a0561db9630483ca27934c6e0ea24b7
出典メモuspto-grants-2010_04