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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710757Generated: November 1, 2026

HCID 11858050, compound → HCID 11858224, compound

https://huagongshe.com/reaction/1710757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11858050HCID 11858050—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11858224HCID 1185822448%

Reaction Steps

A solution of N-(cyclopropylmethyl)-4-methyl-2-{4-[3-(2-methylpyrrolidin-1-yl)propoxy]phenyl}-N-propyl-1,3-oxazole-5-carboxamide 97 (0.25 g, 0.57 mmol, 1 eq) in tetrahydrofuran (15 ml) is treated with borane-tetrahydrofuran complex 1 M in tetrahydrofuran (2.2 ml, 2.2 mmol, 4 eq) and refluxed overnight. The solvent is then removed under reduced pressure and the residue is taken up in ethyl acetate and washed with a saturated solution of aqueous ammonium chloride. The organic layer is dried over magnesium sulfate, filtered and concentrated. The residue is then dissolved in tetrahydrofuran and a 2 N sodium hydroxide solution is added to reach pH 10. The mixture is refluxed for 40 h and a saturated solution of aqueous ammonium chloride is added and the solution extracted two times with ethyl acetate. The organic layers are dried over magnesium sulfate, filtered and concentrated under vacuum. Purification by chromatography over silicagel (eluent: dichloromethane/methanol/ammonia 96/3.6/0.4) gives 0.115 g of N-(cyclopropylmethyl)-N-[(4-methyl-2-{4-[3-(2-methylpyrrolidin-1-yl)propoxy]phenyl}-1,3-oxazol-5-yl)methyl]-N-propylamine 112.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790720B2
Source datasetuspto-grants-2010_09
ORD IDord-18b8cf066dfe42d0a754e4b5f6d02b95
Source noteuspto-grants-2010_09