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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881636Generated: October 25, 2026

2-(4-t-Butylphenyl)-3-hydroxy-4-methylcarbonylthiophene → Methyl 4-{[(2-{1-[5-(4-t-butylphenyl)-4-hydroxy-3-thienyl]ethylidene}hydrazino)carbonothioyl]amino}-2-nitrobenzoate

https://huagongshe.com/reaction/1881636

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-t-Butylphenyl)-3-hydroxy-4-methylcarbonylthiopheneHCID 44207289—
ReactantMethyl 4-hydrazinocarbonothioylamino-2-nitrobenzoateHCID 86014590—
CatalystHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-{[(2-{1-[5-(4-t-butylphenyl)-4-hydroxy-3-thienyl]ethylidene}hydrazino)carbonothioyl]amino}-2-nitrobenzoateHCID 7236003281%

Reaction Steps

Dimethylformamide (1.3 mL) and conc. hydrochloric acid (1 drop) were added to 2-(4-t-butylphenyl)-3-hydroxy-4-methylcarbonylthiophene (71 mg, 0.26 mmol) synthesized in Reference Synthetic Example 33 and methyl 4-hydrazinocarbonothioylamino-2-nitrobenzoate (70 mg, 0.26 mmol) synthesized in Reference Synthetic Example 56, and the mixture was stirred at room temperature for 2 days. The precipitated solid was filtered to obtain 110 mg of the desired product as a pale yellow solid (yield 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318796B2
Source datasetuspto-grants-2012_11
ORD IDord-3e8ccd4483d04ed3822c303a97f8e851
Source noteuspto-grants-2012_11