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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492935Generated: October 30, 2026

Diethyl Ether → HCID 57677399, compound

https://huagongshe.com/reaction/492935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant(1S)-(+)-Camphor-10-sulphonic acidHCID 218580—
ReactantPhenylacetyl isothiocyanateHCID 12454157—
Reactant4-(4-Amino-2-fluorophenoxy)-6-{[4-(1-methylpiperazin-4-yl)piperidin-1-yl]carbonylamino}pyrimidineHCID 23153158—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductHCID 57677399HCID 5767739953.3%

Reaction Steps

4-(4-Methylpiperazin-1-yl)piperidine-1-carboxylic acid [6-(4-amino-2-fluorophenoxy)pyrimidin-4-yl]amide (81 mg) was dissolved in ethanol (1 ml), and then (S)-(+)-10-camphorsulfonic acid (44 mg) was added thereto, followed by stirring for 5 min. A 0.25 M solution of 2-phenylacetyl isothiocyanate in toluene (1.14 ml) was added thereto, followed by stirring for 1 hr. The reaction mixture was partitioned between ethyl acetate (30 ml) and a saturated aqueous solution of sodium hydrogencarbonate (20 ml). The organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate (20 ml), water (20 ml), brine (20 ml) in this order, and dried over anhydrous sodium sulfate. The solvent was evaporated to give a residue, which was then purified by silica gel column chromatography (FUJI Silysia NH, eluent; heptane:ethyl acetate=1:5 to 1:10, then ethyl acetate). Fractions containing the target compound were concentrated under reduced pressure to give a residue, to which diethyl ether (1.5 ml) and hexane (3.0 ml) were then added to suspend. The solid was filtered off, and dried under aeration to provide the titled compound (61.1 mg, 53.3%) as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-ea5de0d518184c5a86d99b394748acb4
Source noteuspto-grants-2009_05