Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965393Generated: October 26, 2026

3-Bromophenol → 8-hydroxy-8-(7-hydroxy-2,3-dihydro-1,4-benzodioxin-6-yl)-6-(4-methoxybenzyl)-6,8-dihydro-7H-[1,3]thiazolo[5,4-e]indol-7-one

https://huagongshe.com/reaction/1965393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromophenolHCID 11563—
Reactant2,3-Dihydro-1,4-benzodioxin-6-olHCID 9115273—
Reactant1-((5-(Trifluoromethyl)furan-2-yl)methyl)indoline-2,3-dioneHCID 67356488—
Reactant6-(4-methoxybenzyl)-6H-[1,3]thiazolo[5,4-e]indole-7,8-dioneHCID 67357746—
Product8-hydroxy-8-(7-hydroxy-2,3-dihydro-1,4-benzodioxin-6-yl)-6-(4-methoxybenzyl)-6,8-dihydro-7H-[1,3]thiazolo[5,4-e]indol-7-oneHCID 67356923—

Reaction Steps

Following the procedure as described in PREPARATION 2A and making non-critical variations using 2,3-dihydrobenzo[b][1,4]dioxin-6-ol to replace 3-bromophenol, and 6-(4-methoxybenzyl)-6H-[1,3]thiazolo[5,4-e]indole-7,8-dione to replace 1-((5-(trifluoromethyl)furan-2-yl)methyl)indoline-2,3-dione, 8-hydroxy-8-(7-hydroxy-2,3-dihydro-1,4-benzodioxin-6-yl)-6-(4-methoxybenzyl)-6,8-dihydro-7H-[1,3]thiazolo[5,4-e]indol-7-one was obtained (39%) as a colorless solid: MS (ES+) m/z 477.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415370B2
Source datasetuspto-grants-2013_04
ORD IDord-4ef73e1c4d7f42529239f9eafbbf4f4d
Source noteuspto-grants-2013_04