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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855673Generated: October 30, 2026

Diisopropylethylamine → HCID 178468423, compound

https://huagongshe.com/reaction/1855673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant1-{1-[(R)-2-amino-3-(4-methoxyphenyl)propionyl]-4-cyclohexylpiperidin-4-yl}butan-1-oneHCID 66987681—
ReactantHCID 178510967HCID 178510967—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 178468423HCID 17846842313.7%

Reaction Steps

16 μL of diisopropylethylamine and 10 mg (51 μmol) of 4-nitrophenyl chloroformate are added to 25 mg (47 μmol) of 1-{1-[(R)-2-amino-3-(4-methoxyphenyl)propionyl]-4-cyclohexylpiperidin-4-yl}butan-1-one (cf. preparation 4.4) dissolved in 5 ml of DCM. The reaction mixture is stirred for 2 hours at room temperature. The reaction is stopped by adding water and the organic compounds are extracted with DCM. The organic phase is then dried over MgSO4, filtered and concentrated. The oil obtained is dissolved in 5 ml of DMF at 80° C., and 14 mg of 5-(1H-imidazol-4-yl)pentylamine bis(trifluoroacetate) are added. The reaction mixture is stirred at 80° C. for 5 minutes and for 18 hours at room temperature. The organic phase is washed with 1N sodium hydroxide, extracted with dichloromethane and then dried over MgSO4, filtered and concentrated. The crude product obtained is purified by preparative HPLC. 3 mg of ethyl 4-cyclohexyl-1-[(R)-2-{3-[5-(1H-imidazol-4-yl)pentyl]ureido}-3-(4-methoxy-phenyl)propionyl]piperidine-4-carboxylate are obtained in a yield of 10%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962846B2
Source datasetuspto-grants-2015_02
ORD IDord-8d5ec75034094f21a684d0e42cbc57cf
Source noteuspto-grants-2015_02