Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360556Generated: October 30, 2026

Carbonate Ion → N-(4-{[(4-aminobiphenyl-3-yl)amino]carbonyl}phenyl)-7-benzyl-2,7-diazaspiro[4.4]nonane-2-carboxamide

https://huagongshe.com/reaction/2360556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbonate IonHCID 19660—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Isocyanatobenzoyl chlorideHCID 2733323—
Reactant2-Benzyl-2,7-diazaspiro[4.4]nonaneHCID 42614542—
ReactantN-(3-Amino[1,1'-biphenyl]-4-yl)-carbamic Acid tert-Butyl EsterHCID 57717454—
SolventDichloromethaneHCID 6344—
ProductN-(4-{[(4-aminobiphenyl-3-yl)amino]carbonyl}phenyl)-7-benzyl-2,7-diazaspiro[4.4]nonane-2-carboxamideHCID 24746278—

Reaction Steps

To a solution of stirring 4-isocyanatobenzoyl chloride (50 mg, 0.275 mmol) in 3 mL of dichloromethane was added 2-benzyl-2,7-diazaspiro[4,4]nonane (60 mg, 0.275 mmol) slowly over a period of 10 minutes. The reaction mixture was allowed to stir for 30 min. at room temperature. Tert-butyl (3-aminobiphenyl-4-yl)carbamate (78.2 mg, 0.275 mmol) was then added, followed by the addition of diisopropylethylamine (48 μL, 0.275 mmol). The reaction mixture was allowed to stir for 1 hour at room temperature. Argonaut MP-Carbonate scavenging resin (285 mg, 0.825 mmol) was then added and stirred overnight at room temperature. The mixture was then filtered from scavenging resin and concentrated. Added dichloromethane (1 mL) and stirred, then treated with trifluoroacetic acid (1 mL). The reaction mixture was concentrated after 2 hours of stirring at room temperature and the crude residue was purified by reverse-phase chromatography (5-50-95% acetonitrile/water with 0.1% formic acid). The appropriate fractions were combined and lyophilized. MS (ESI+): cal'd [M+H]+ 546.3, obs'd 546.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686020B2
Source datasetuspto-grants-2014_04
ORD IDord-ad55c15e99aa435fbc3058880bd708b7
Source noteuspto-grants-2014_04