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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281192Generated: November 1, 2026

1,2-Dichloroethane → HCID 23382062, compound

https://huagongshe.com/reaction/1281192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantN-(Methoxycarbonyl)-L-tert-leucineHCID 11263950—
Reactant1-[p-(4-methylpiperazin-1-yl)phenyl]-4(S)-hydroxy-2-amino-5(S)-[N-(N-methoxycarbonyl-(L)-valyl)amino]-6-phenyl-2-azahexaneHCID 23382084—
SolventDimethylformamideHCID 6228—
SolventEthanol ethylacetateHCID 21584252—
ProductHCID 23382062HCID 23382062—

Reaction Steps

129 mg (0.68 mmol) of N-methoxycarbonyl-(L)-tert-leucine, 244 mg (1.28 mmol) of EDC and 115 mg (0.85 mmol) of HOBT are initially introduced, under a N2 atmosphere, in 5.4 ml of DMF. After 20 min at RT, 0.355 ml (2.55 mmol) of triethylamine is added. 232 mg (0.425 mmol) of 1-[p-(4-methylpiperazin-1-yl)phenyl]-4(S)-hydroxy-2-amino-5(S)-[N-(N-methoxycarbonyl-(L)-valyl)amino]-6-phenyl-2-azahexane (Example 16g) are then added and the mixture is thoroughly stirred overnight; working-up then takes place in analogy with Example 16. Column chromatography (SiO2; ethyl acetate/ethanol 1:1) results in the title compound:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451973B1
Source datasetuspto-grants-2002_09
ORD IDord-c31087e738884239bc95be2478db82b3
Source noteuspto-grants-2002_09