HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289565Generated: October 31, 2026
HCID 18697866, compound → HCID 18697752, compound
https://huagongshe.com/reaction/2289565
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18697866 | HCID 18697866 | — |
| Reactant | HCID 18697913 | HCID 18697913 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18697752 | HCID 18697752 | 26.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06093714 |
|---|
| Source dataset | uspto-grants-2000_07 |
|---|
| ORD ID | ord-226af01a2e784774ba986978c17cc0cc |
|---|
| Source note | uspto-grants-2000_07 |
|---|