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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242827Generated: November 2, 2026

6-Bromoindole → HCID 11336128, compound

https://huagongshe.com/reaction/2242827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-BromoindoleHCID 676493—
ReactantHCID 21072606HCID 21072606—
ProductHCID 11336128HCID 11336128—

Reaction Steps

The product of Example 2A (300 mg, 0.8 mmol) was coupled with 6-bromoindole (Aldrich, 196 mg, 1 mmol) according to the procedure in 2B. The title compound was purified by chromatography (SiO2, CH2Cl2:MeOH:NH3.H2O, 90:10:1, Rf. 0.20) as a solid (30 mg, yield, 12%). 1H NMR (300 MHz, CD3OD) δ 1.45-1.58 (m, 1H), 1.64-1.90 (m, 2H), 2.01-2.15 (m, 1H), 2.17-2.24 (m, 1H), 2.75-3.04 (m, 5H), 3.30-3.42 (m, 1H), 4.53-4.61 (m, 1H), 6.43 (dd, J=3.1, 0.7 Hz, 1H), 6.97 (dt, J=8.8, 2.6 Hz, 2H), 7.21-7.27 (m, 2H), 7.52-7.60 (m, 4H) ppm. MS (DCI/NH3): m/z 319 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674794B2
Source datasetuspto-grants-2010_03
ORD IDord-84a94b8a6d264da9814c314b32f3ba58
Source noteuspto-grants-2010_03