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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444994Generated: October 30, 2026

Diisopropylethylamine → 17-[Benzyloxycarbonylmethyl-(2-tert-butoxycarbonyl-ethyl)-carbamoyl]-heptadecanoic acid tert-butyl ester

https://huagongshe.com/reaction/444994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant3-(Benzyloxycarbonylmethylamino)propionic acid tert-butyl esterHCID 58020928—
Reactant1-tert-Butyl 18-(2,5-dioxopyrrolidin-1-yl) octadecanedioateHCID 58249213—
SolventDimethylformamideHCID 6228—
Product17-[Benzyloxycarbonylmethyl-(2-tert-butoxycarbonyl-ethyl)-carbamoyl]-heptadecanoic acid tert-butyl esterHCID 6672459485%

Reaction Steps

3-(Benzyloxycarbonylmethylamino)propionic acid tert-butyl ester (0,030 g, 0.1 mmol) and octadecanedioic acid tert-butyl ester 2,5-dioxo-pyrrolidin-1-yl ester (0,050 mg, 0.1 mmol) was suspended in dry DMF (1 ml). HOAt (0.014 g, 0.1 mmol) and DIPEA (0.21 ml, 1.2 mmol) was added. The yellow reaction mixture was stirred under nitrogen for 42 h. The reaction mixture was concentrated. The residue was redissolved in EtOAc and washed with 0.1 N HCl (2×), water (1×), dried (Na2SO4) and concentrated to give 17-[Benzyloxycarbonylmethyl-(2-tert-butoxycarbonyl-ethyl)-carbamoyl]-heptadecanoic acid tert-butyl ester in 85% yield (55 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476228B2
Source datasetuspto-grants-2013_07
ORD IDord-5fea51556fca4b77bdc9a40ae74cf5e9
Source noteuspto-grants-2013_07