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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892470Generated: October 28, 2026

1,1'-Carbonyldiimidazole → 4-{2-[2-(Acetylamino)-1,3-thiazol-4-yl]ethyl}phenyl tert-butyl hydrazine-1,2-dicarboxylate

https://huagongshe.com/reaction/1892470

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactanttert-Butyl carbazateHCID 70091—
ReactantN-{4-[2-(4-hydroxyphenyl)ethyl]-1,3-thiazol-2-yl}acetamideHCID 86649977—
SolventTetrahydrofuranHCID 8028—
Product4-{2-[2-(Acetylamino)-1,3-thiazol-4-yl]ethyl}phenyl tert-butyl hydrazine-1,2-dicarboxylateHCID 8664997850.1%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of N-{4-[2-(4-hydroxyphenyl)ethyl]-1,3-thiazol-2-yl}acetamide (655.8 mg, 2.50 mmol) in anhydrous tetrahydrofuran (12 ml) was added 1,1′-carbonyldiimidazole (608.1 mg, 3.75 mmol). After stirring at 45° C. for 1 hr, the mixture was cooled to room temperature. tert-Butyl carbazate (495.6 mg, 3.75 mmol) was added, and the mixture was stirred at room temperature for 15 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (FUJI SILYSIA CHEMICAL LTD. BW-300SP 80 g, ethyl acetate:hexane=1:1→3:2) and chemically modified silica gel column chromatography (FUJI SILYSIA CHEMICAL LTD. DM-2035 45 g, dichloromethane:methanol=50:1→20:1) to give 4-{2-[2-(acetylamino)-1,3-thiazol-4-yl]ethyl}phenyl tert-butyl hydrazine-1,2-dicarboxylate (526.4 mg, 1.252 mmol, yield 50.0%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507690B2
Source datasetuspto-grants-2013_08
ORD IDord-3a66605e2c9245dabcf0c70e190a4e5d
Source noteuspto-grants-2013_08