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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602500Generated: October 30, 2026

HCID 54318654, compound → HCID 19611331, compound

https://huagongshe.com/reaction/1602500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54318654HCID 54318654—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19611331HCID 1961133143%

Reaction Steps

Ethyl 2-[3-[(4-tert-butyl-2-thiazolyl)methoxy]-5-(4-nitrobenzyloxycarbonylamino)benzoylamino]-4-[3-(4-chlorophenylsulfonyl)propyl]phenoxyacetate (0.50 g, 0.57 mmol) was dissolved in a mixed solution of ethanol (10 ml) and tetrahydrofuran (10 ml), 10% palladium-carbon (0.10 g) was added to the solution, and the mixture was stirred at room temperature for 3 hours in an atmosphere of hydrogen. The reaction solution was filtered and the resulting filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent=acetone:chloroform=3:100) and crystallized from acetonitrile to give ethyl 2-[3-amino-5-[(4-tert-butyl-2-thiazolyl)methoxy]benzoylamino]-4-[3-(4- chlorophenylsulfonyl)propyl]phenoxyacetate (0.17 g, 0.24 mmol, 43%) as light yellow crystals. Its structure is shown in Table 30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981559
Source datasetuspto-grants-1999_11
ORD IDord-c6a393af506b474cac88e0d4bc9e4c0a
Source noteuspto-grants-1999_11