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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260550Generated: October 27, 2026

Ethyl Acetate → N-(4-(4-(6-isopropoxypyridazin-3-yloxy)phenyl)butan-2-yl)acetamide

https://huagongshe.com/reaction/1260550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant3-Chloro-6-isopropoxypyridazineHCID 252823—
ReactantN-[3-(4-Hydroxyphenyl)-1-methylpropyl]acetamideHCID 59956161—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-(4-(4-(6-isopropoxypyridazin-3-yloxy)phenyl)butan-2-yl)acetamideHCID 49858288—

Reaction Conditions

Temperature150 °C

Reaction Steps

N-[3-(4-Hydroxyphenyl)-1-methylpropyl]acetamide (311 mg, 1.5 mmol) was dissolved in 3 ml of NMP, admixed with sodium hydride (55% in oil) (120 mg, 3 mmol) and, after addition of 3-chloro-6-isopropoxypyridazine (259 mg, 1.5 mmol) stirred in a microwave reactor at 150° C. for 15 min. Following addition of ethyl acetate and water, the organic phase was separated off, concentrated and purified by preparative HPLC (PR18, acetonitrile/water 0.1% TFA). Yield: 40mg (8%), M+H+: 344.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470841B2
Source datasetuspto-grants-2013_06
ORD IDord-29f8be87b45d4bdb9e589d83e2752d15
Source noteuspto-grants-2013_06