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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234131Generated: October 26, 2026

Diisopropylethylamine → HCID 178501777, compound

https://huagongshe.com/reaction/234131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantDi(succinimido) carbonateHCID 676246—
ReactantHCID 131719797HCID 131719797—
ReactantHCID 178453624HCID 178453624—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
ProductHCID 178501777HCID 178501777—

Reaction Steps

To the solution of 877 mg (3.41 mmol) of the compound prepared in (a) (3.41 mmole) in the mixture of 6.8 ml of dimethylformamide and 1.4 ml of pyridine were added 874 mg of N,N'-disuccinimidyl carbonate and a catalytic amount of 4-dimethylaminopyridine, and the resulting mixture was stirred at room temperature for 3 hours, whereafter 1.45 g of the compound prepared in (b) and 0.59 ml of N,N-diisopropylethylamine were added. The mixture was further stirred at room temperature overnight. After the reaction mixture was concentrated under reduced pressure, the resulting solid product was purified by column chromatography on silica gel. The solid product thus obtained was washed with ether to give 1.1 g of dimethyl [[4-[[[trans-4-(t-butyloxycarbonylaminomethyl)cyclohexyl]carbonylamino]acetyl]-o-phenylene]dioxy]diacetate as pale yellow crystals (yield, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594004
Source datasetuspto-grants-1997_01
ORD IDord-462c1188d1284c88963a6dabc3462030
Source noteuspto-grants-1997_01