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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301844Generated: October 31, 2026

4-t-butyldimethylsilyloxy-N2-(4-t-butylbenzoyl)-1,2-benzenediamine → 4-t-Butyldimethylsilyloxy-N2-(4-t-butylbenzoyl)-N1-(3-bromoindol-6-ylcarbonyl)-1,2-benzenediamine

https://huagongshe.com/reaction/2301844

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-t-butyldimethylsilyloxy-N2-(4-t-butylbenzoyl)-1,2-benzenediamineHCID 11795190—
Reactant3-Bromo-1H-indole-6-carboxylic acidHCID 15543043—
Product4-t-Butyldimethylsilyloxy-N2-(4-t-butylbenzoyl)-N1-(3-bromoindol-6-ylcarbonyl)-1,2-benzenediamineHCID 5373951879%

Reaction Steps

Using the procedure described in Example 9, Part C, 4-t-butyldimethylsilyloxy-N2-(4-t-butylbenzoyl)-1,2-benzenediamine (750 mg, 1.9 mmol) and 3-bromoindole-6-carboxylic acid (456 mg, 1.9 mmol) yielded 930 mg (79%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500851B2
Source datasetuspto-grants-2002_12
ORD IDord-4d957149532942c1acc5bc442eeef421
Source noteuspto-grants-2002_12