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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393520Generated: October 30, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 503192, compound

https://huagongshe.com/reaction/2393520

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 503167HCID 503167—
ReactantLithiumHCID 3028194—
ReactantHCID 54304856HCID 54304856—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 503192HCID 503192161.8%
ProductHCID 22870891HCID 22870891—

Reaction Steps

N-tert-butyl-1-{3(S)-amino-2(R)-hydroxy-4-phenylbutyl}-4(R)-phenylpiperidine-2(S)-carboxamide {prepared by hydrogenolysis (5% Pd/C, 1 atmosphere, MeOH, 2h) from 0.605 mg (0.108 mmol) of N-tert-butyl-1-{3(S)-(benzyloxycarbonylamino)-2(R)-hydroxy-4-phenylbutyl}-4(R)-phenylpiperidine-2(S)-carboxamide (see entry 1 of Table I)} was dissolved in DMF (1.6 mL). The lithium salt of N-{(2-pyridinylmethoxy)carbonyl}isoleucine (586 mg, 0.228 mmol), 1-hydroxybenzotriazole (32 mg, 0.237 mmol) and N-ethyl-N'-{3-(dimethylamino)propyl}carbodiimide (45.4 mg, 0.237 mmol) were added to the solution. The mixture was stirred at room temperature for 18 h. Thereafter, the reaction mixture was diluted with Et2O, washed with H2O , a saturated aqueous solution of NaHCO3 (2×) and brine, dried (MgSO4) and evaporated to dryness. The resulting yellow oil was purified by flash chromatography (SiO2, eluent: CHCl3, MeOH, 97.5:2.5 and then 95:5) to give the title compound as a white solid (58.7 mg). FAB mass spectrum, m/z: 672 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807870
Source datasetuspto-grants-1998_09
ORD IDord-72407488692b4dcf8e281b4ca29f15c9
Source noteuspto-grants-1998_09