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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215865Generated: October 29, 2026

Diisopropylamine → HCID 21951863, compound

https://huagongshe.com/reaction/2215865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantBenzene, 1-isocyanato-4-nitro-HCID 66012—
ReactantMethyl 2-amino-4-[(tert-butoxycarbonyl)amino]benzoateHCID 21056495—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 21951863HCID 2195186347.2%

Reaction Steps

A solution of 2-amino-4-(tert-butoxycarbonylamino)-benzoic acid methyl ester (6.3 g, 23.6 mmol) and 4-nitrophenyl isocyanate (7.8 g, 47.4 mmoles) in 100 mL dry dimethylformamide was stirred at room temperature for 20 hrs. To it was then added diisopropylamine (8.2 mL, 47.4 mmol), and the reaction mixture was heated in 80° C. bath for 2 hrs. It was cooled to room temperature and the solid precipitates were filtered off. The dimethylformamide filtrate was concentrated in vacuo to evaporate the solvent. To the residue was added 400 mL dichloromethane. After stirred and swirled, the solid was isolated by filtration. This solid was then dissolved in 100 mL dimethylformamide and 200 mL methanol. To it was added 1.0 g 10% Pd/C, and the mixture was subjected to standard hydrogenation using a balloon for 20 hrs. It was filtered through a celite bed. The filtrate was concentrated in vacuo and purified using flash column to afford the title compound (4.1 g, 44%). ES+ MS showed 397 m/z, the correct mass for the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109332B2
Source datasetuspto-grants-2006_09
ORD IDord-7b59d108aac445f49dbbb089cdb00bd4
Source noteuspto-grants-2006_09