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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356362Generated: November 1, 2026

Aniline → HCID 22396897, compound

https://huagongshe.com/reaction/1356362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantHCID 22396611HCID 22396611—
ReactantSodium t-butoxideHCID 23676156—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 22396897HCID 22396897—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of tert-butyl 10-bromo-1,4,5,6-tetrahydroazepino[4,5-b]indole-3(2H)-carboxylate (600 mg), sodium t-butoxide (220 mg), tris(dibenzylideneacetone) dipalladium (23 mg), aniline (183 mg) toluene (1.64 ml) was added 2-(di-t-butylphosphino)biphenyl (30 mg) and the reaction mixture was heated at 50° C. The reaction mixture stirred 16 h, was poured into brine, extracted with CH2Cl2, dried over MgSO4, filtered and concentrated. The crude product was stirred in CH2Cl2 (8 ml) and TFA (2 ml) was added. The reaction mixture stirred 1 h, was quenched with 2N NaOH, extracted with CH2Cl2, dried over MgSO4, filtered and concentrated. Purification via flash chromatography (silica gel, CH2Cl2/MeOH, 9/1 with 0.5% NH4OH) provided the title compound: 1H NMR (DMSO-d6) δ 2.68, 2.83-2.90, 6.58-6.67, 6.89, 7.06, 7.54, 10.71.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586421B2
Source datasetuspto-grants-2003_07
ORD IDord-b385ddce34bc410ba8a6e9586449e7ef
Source noteuspto-grants-2003_07