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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289565Generated: October 31, 2026

HCID 18697866, compound → HCID 18697752, compound

https://huagongshe.com/reaction/2289565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18697866HCID 18697866—
ReactantHCID 18697913HCID 18697913—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 18697752HCID 1869775226.4%

Reaction Steps

To a solution of the 1:1 mixture (872 mg) of ethyl 4-(4-t-butoxycarbonylamino-2-nitrobenzoyl)-1-(4-methoxybenzyl)-1,2,3-triazole-5-carboxylate and ethyl 5-(4-t-butoxycarbonylamino-2-nitrobenzoyl)-1-(4-methoxybenzyl)-1,2,3-triazole-4-carboxylate, prepared in the step (b), in ethyl acetate (20 ml) was added 10% palladium on carbon (30 mg). The mixture was stirred under a hydrogen atmosphere overnight and filtered. The filtrate was concentrated under reduced pressure, and the resulting oil was purified by column chromatography on silica gel (toluene:ethyl acetate=2:1) to give ethyl 4-(2-amino-4-t-butoxycarbonylaminobenzoyl)-1-(4-methoxybenzyl)-1,2,3-triazole-5-carboxylate (c-1: less polar component (LP)) (217 mg) and a mixture (219 mg) of the compound c-1 and ethyl 5-(2-amino-4-t-butoxycarbonylaminobenzoyl)-1-(4-methoxybenzyl)-1,2,3-triazole-4-carboxylate (c-2: more polar component (MP)) (219 mg). c-1 (LP):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093714
Source datasetuspto-grants-2000_07
ORD IDord-226af01a2e784774ba986978c17cc0cc
Source noteuspto-grants-2000_07