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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044096Generated: November 1, 2026

Methanol → HCID 57489647, compound

https://huagongshe.com/reaction/2044096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium AcetateHCID 517165—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57489644HCID 57489644—
CatalystTitanium isopropoxideHCID 11026—
SolventDimethylformamideHCID 6228—
ProductHCID 57489647HCID 574896478.7%

Reaction Steps

A solution of 5-fluoro-2-(4-morpholinophenylamino)-6-(3-oxocyclohex-1-enyl)nicotinamide (1.2 g, 2.92 mmol), ammonium acetate (2.254 g, 29.2 mmol) and titanium(IV) isopropoxide (2.57 mL, 8.77 mmol) in DMF (0.8 mL) was stirred at rt overnight. To the above solution were added sodium borohydride (0.221 g, 5.85 mmol) and 0.2 mL of MeOH. Violent bubbling occurred and the reaction mixture became warm. The reaction mixture was stirred at rt for 1 h. To the reaction mixture was added 1N NaOH (10 mL). A precipitate formed and was filtered through CELITE®, washed with a mixture of methylene chloride, and MeOH (50% each cosolvent) many times until the filter cake was white. The filtrate was washed with water; the aqueous fraction was back extracted 3 times with methylene chloride. The combined organic fractions were concentrated and the residue was purified by MPLC (ISCO, 5%-20% gradient ammonia/methanol/methylene chloride, 40 g silica gel column) to yield 105 mg of product as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586751B2
Source datasetuspto-grants-2013_11
ORD IDord-dc4b3d510578419f84870906be12e96c
Source noteuspto-grants-2013_11