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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714119Generated: November 2, 2026

Morpholine → Bavisant

https://huagongshe.com/reaction/1714119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(4-Cyclopropyl-piperazine-1-carbonyl)-benzaldehydeHCID 59218183—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductBavisantHCID 16061509—

Reaction Conditions

Temperature10 °C

Reaction Steps

To a solution of 4-(4-cyclopropyl-piperazine-1-carbonyl)-benzaldehyde (56.0 g) in 1,2-dichloroethane (550 mL) was added morpholine (37.8 mL) dropwise over 5 min. The mixture was cooled to 10° C. and was treated with NaBH(OAc)3 (64.3 g) in portions over 1 h. After a further 2 h, the mixture was warmed to room temperature, and a water bath was used to keep the temperature below 20° C. After 18 h, water (60 mL) was added while the temperature was kept under 20° C. by the addition of small amounts of ice. After 20 min, the mixture was basified to pH ˜10 with 1 N NaOH (450 mL) and the mixture was stirred for 10 min. The layers were separated, and the organic layer was washed with 1 N NaOH (150 mL). The combined aqueous layers were extracted with CH2Cl2 (200 mL). The combined organic layers were washed with brine (200 mL), dried (Na2SO4), and concentrated to yield the title compound as pale yellow viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795426B2
Source datasetuspto-grants-2010_09
ORD IDord-3ec8365e4fc74a3bbb64cf8976b33c22
Source noteuspto-grants-2010_09