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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900461Generated: October 29, 2026

Potassium Iodide → HCID 178429922, compound

https://huagongshe.com/reaction/900461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium hydrideHCID 24758—
ReactantMorpholine, 4-(2-chloroethyl)-, hydrochloride (1:1)HCID 77210—
ReactantHCID 178429921HCID 178429921—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178429922HCID 178429922—

Reaction Conditions

Temperature180 °C

Reaction Steps

A microwave reaction vial was charged with the title compound of Example 3 [2-(trans-4-Hydroxy-cyclohexylamino)-4-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-indazol-1-yl)-benzamide] (100 mg, 0.244 mmol), 4-(2-chloroethyl)morpholine hydrochloride (45.4 mg, 0.244 mmol), sodium hydride (17.3 mg, 0.732 mmol), and a catalytic amount of potassium iodide. After suspending in DMF, the reaction mixture was heated to 180° C. in the “Personal Chemistry” microwave for eight minutes. The solution was then diluted with water and extracted into EtOAc (2×). The organic layers were extracted with 2N HCl (2×). The aqueous extracts basified with aqueous sodium hydroxide, and were extracted with EtOAc (3×). The combined organics were dried over Na2SO4, concentrated, and purified by column chromatography (EtOAc/MeOH) to yield the title compounds as a white solid. LCMS m/z: (M+H) 523.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07358370B2
Source datasetuspto-grants-2008_04
ORD IDord-c46d48437ed74d05a6a8993f7a82a6b8
Source noteuspto-grants-2008_04