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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423296Generated: October 29, 2026

Chlorosuccinimide → 3-Chloro-5-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indole

https://huagongshe.com/reaction/423296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant5-(3-Chloro-4-isopropoxyphenyl)-3-(1H-indol-5-yl)-1,2,4-oxadiazoleHCID 59318353—
SolventDichloromethaneHCID 6344—
Product3-Chloro-5-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1H-indoleHCID 5931836112.8%

Reaction Steps

D5 (300 mg) and NCS (113 mg) were dissolved in DCM (4.2 ml) and stirred overnight at room temperature. The reaction mixture was then diluted with DCM and washed with H2O. The aqueous solution was extracted with two further portions of DCM and the combined organic solutions were evaporated to dryness. The crude product was triturated with methanol to give the title compound (42 mg) as a brown solid. The methanol was then evaporated and the resultant brown solid triturated with DCM to give a second batch of the title compound (205 mg) as a brown solid. δH (d6-DMSO, 400 MHz): 1.37 (6H, d), 4.89 (1H, septet), 7.45 (1H, d), 7.62 (1H, d), 7.70 (1H, s), 7.93 (1H, d), 8.15 (1H, d), 8.24 (1H, s), 8.25 (1H, s), 11.77 (1H, s). MS (ES): C19H1535Cl2N3O2 requires 387; found 388 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101775B2
Source datasetuspto-grants-2012_01
ORD IDord-92ca3f489b7b4e9d8109c6984cb2658d
Source noteuspto-grants-2012_01