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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027187Generated: October 29, 2026

Water → tert-butyl 3-((6-(2-methoxy-4-(1H-pyrazol-1-yl)phenyl)pyridazin-3-yl)oxy)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1027187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Boc-3-pyrrolidinolHCID 4416939—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3-Chloro-6-[2-methoxy-4-(1H-pyrazol-1-yl)phenyl]pyridazineHCID 86710544—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 3-((6-(2-methoxy-4-(1H-pyrazol-1-yl)phenyl)pyridazin-3-yl)oxy)pyrrolidine-1-carboxylateHCID 86710583100%

Reaction Conditions

Temperature50 °C

Reaction Steps

Potassium tert-butoxide (1.0 M in THF, 0.98 mL, 0.98 mmol) was added to tert-butyl 3-hydroxypyrrolidine-1-carboxylate (0.18 g, 0.98 mmol) in THF (3.3 mL) at 0° C. and the mixture was stirred for 10 min at 50° C. 3-Chloro-6-(2-methoxy-4-(1H-pyrazol-1-yl)phenyl)pyridazine Intermediate 2-1 (0.12 g, 0.40 mmol) was added to the reaction at 0° C. and the mixture was stirred for 2 h at RT. Water (0.1 mL) was added and the solvent was concentrated under reduced pressure to afford (0.18 g, 100%) of a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729263B2
Source datasetuspto-grants-2014_05
ORD IDord-fa0bac9cbb4b48d389a577def4324bdf
Source noteuspto-grants-2014_05