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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355726Generated: November 1, 2026

1-Hydroxybenzotriazole → (5-Bromo-2,4-Dihydroxyphenyl)(1,3-Dihydro-2h-Isoindol-2-Yl)methanone

https://huagongshe.com/reaction/2355726

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant5-Bromo-2,4-dihydroxybenzoic acidHCID 81814—
ReactantIsoindolineHCID 422478—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDimethylformamideHCID 6228—
Product(5-Bromo-2,4-Dihydroxyphenyl)(1,3-Dihydro-2h-Isoindol-2-Yl)methanoneHCID 1594223444%

Reaction Steps

A solution of 5-bromo-2,4-dihydroxy-benzoic acid (520 mg, 2.33 mmol) in DMF (5 mL) was treated with 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (471 mg, 2.45 mmol) then HOBt (362 mg, 2.68 mmol). After 25 min. 2,3-dihydro-1H-isoindole (0.5 mL, 2.63 mmol) was added then the mixture was stirred at r.t. for 18 h. The solvent was removed in vacuo then the residue was taken up in ethyl acetate and washed with 1N hydrochloric acid, saturated sodium bicarbonate solution and brine then dried (MgSO4) and concentrated. The residue was triturated with methanol to afford the title compound as a grey solid (328 mg, 44%). 1H NMR (DMSO-d6) 10.45 (1H, s), 10.32 (1H, s), 7.36 (1H, br.s), 7.35 (1H, s), 7.28 (3H, br.s), 6.59 (1H, s), 4.77 (2H, br.s), 4.71 (2H, br.s). MS: [M+H]+ 332/334.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754725B2
Source datasetuspto-grants-2010_07
ORD IDord-d1ec6de8c5ae4445985f88dedaecc873
Source noteuspto-grants-2010_07