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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402042Generated: October 26, 2026

Acetic Acid → tert-butyl 3-(5-(5-chloro-2-hydroxyphenyl)-1H-pyrazol-1-yl)azetidine-1-carboxylate

https://huagongshe.com/reaction/1402042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant(E)-1-(5-chloro-2-hydroxyphenyl)-3-(dimethylamino)prop-2-en-1-oneHCID 33728788—
ReactantTert-butyl 3-hydrazinylazetidine-1-carboxylateHCID 58042291—
SolventEthanolHCID 702—
Producttert-butyl 3-(5-(5-chloro-2-hydroxyphenyl)-1H-pyrazol-1-yl)azetidine-1-carboxylateHCID 136063615—

Reaction Conditions

Temperature0 °C

Reaction Steps

Tert-butyl 3-hydrazinoazetidine-1-carboxylate, (Preparation 696, 88.37 g, 0.4247 mol) was dissolved in ethanol (883.7 mL) and the solution was cooled to 0° C. in an ice bath. Acetic acid (97.36 mL, 1.70 mol) was added followed by (2E)-1-(5-chloro-2-hydroxyphenyl)-3-(dimethylamino)prop-2-en-1-one, (Preparation 852, 95.86 g, 0.4247 mol) and the resulting slurry was allowed to warm to room temperature then stirred at room temperature for 2 days. The resulting suspension was cooled to 0° C. and the solid was filtered off, washed with cold ethanol (2×40 mL) and dried to give the title compound as a white granular solid, (83.23 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907101B2
Source datasetuspto-grants-2014_12
ORD IDord-badfbd94ce2049979f8de948c2884588
Source noteuspto-grants-2014_12