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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581995Generated: October 30, 2026

Aniline → N-phenyl-2-(tert-butoxycarbonylamino)-5-indan carboxamide

https://huagongshe.com/reaction/1581995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant2-((tert-butoxycarbonyl)amino)-2,3-dihydro-1H-indene-5-carboxylic acidHCID 22719598—
SolventDichloromethaneHCID 6344—
ProductN-phenyl-2-(tert-butoxycarbonylamino)-5-indan carboxamideHCID 2271964670%

Reaction Steps

Using 2-(tert-butoxycarbonylamino)-5-carboxyindan (30 mg, 0.11 mmol) synthesized in Preparation Example 4, aniline (21 μl, 0.23 mmol), triethylamine (0.20 ml, 1.4 mmol), propanephosphonic acid anhydride (0.3 ml), dimethylaminopyridine (a catalytic amount) and methylene chloride (0.25 ml), a similar procedure to a) in Example 29 was carried out. The product obtained was purified by silica gel chromatography (hexane:ethyl acetate=4:1 to 7:3) to obtain N-phenyl-2-(tert-butoxycarbonylamino)-5-indan carboxamide (27 mg, 0.077 mmol) having the following physical properties:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734180B1
Source datasetuspto-grants-2004_05
ORD IDord-2a83afdec58f4a3689ea6b09cdb0a145
Source noteuspto-grants-2004_05