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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423355Generated: October 25, 2026

1,2-Dichloroethane → HCID 59318425, compound

https://huagongshe.com/reaction/423355

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant3-Bromo-4-methoxybenzoic acidHCID 66836—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactantethyl 3-[3-chloro-5-[(Z)-N'-hydroxycarbamimidoyl]indol-1-yl]propanoateHCID 178471837—
SolventDimethylformamideHCID 6228—
ProductHCID 59318425HCID 59318425—

Reaction Conditions

Temperature80 °C

Reaction Steps

The 3-bromo-4-(methyloxy)benzoic acid (commercial: ICN) (243 mg, 1.05 mmol) stirring in DMF (10 ml) was treated with EDC (219 mg, 0.1.14 mmol) followed by HOBt (156 mg, 0.1.14 mmol). The resultant solution was stirred for 10 minutes. Added ethyl 3-{3-chloro-5-[(hydroxyamino)(imino)methyl]-1H-indol-1-yl}propanoate (D96) (324 mg, 1.05 mmol) and stirred at RT for 45 minutes. The solution was heated at 80° C. for 4 hours then left standing overnight. The solution was heated at 80° C. for a further 4 hours to give one major product. Evaporated off the DMF, added EtOAc (50 ml) and washed with water (50 ml). The EtOAc was washed with sat. aqueous sodium hydrogen carbonate (50 ml) and water (50 ml) then dried over MgSO4. Evaporated off the solvent and crystallised from ethanol to yield the title compound as 280 mg of cream solid. δH (400 MHz, d6-DMSO) 1.10 (3H, t), 2.90 (2H, t), 3.99-4.05 (5H, m), 4.49 (2H, t), 7.38 (1H, d), 7.74 (1H, s), 7.80 (1H, d), 7.97 (1H, d), 8.21-8.23 (2H, m), 8.36 (1H, d). MS (ES) C22H1981Br35ClN3O4 requires 505; found 506 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101775B2
Source datasetuspto-grants-2012_01
ORD IDord-cf322d11f21f4b97bf8c87d2e910d806
Source noteuspto-grants-2012_01