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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350260Generated: November 1, 2026

Acetic Acid → (3R)-N-(benzyloxy)-6-cyclohexyl-3-{4-[(isopropylamino)methyl]-1,3-oxazol-2-yl}hexanamide

https://huagongshe.com/reaction/1350260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDichloromethaneHCID 6344—
ReactantIsopropylamineHCID 6363—
Reactant(3R)-N-(benzyloxy)-6-cyclohexyl-3-(4-formyl-1,3-oxazol-2-yl)hexanamideHCID 60077589—
Product(3R)-N-(benzyloxy)-6-cyclohexyl-3-{4-[(isopropylamino)methyl]-1,3-oxazol-2-yl}hexanamideHCID 2130502432%

Reaction Steps

A solution of (3R)-N-(benzyloxy)-6-cyclohexyl-3-(4-formyl-1,3-oxazol-2-yl)hexanamide (preparation 156) (200 mg, 0.50 mmol) in DCM (10 ml) was treated with isopropylamine (43 μl, 0.50 mmol) and stirred at room temperature for 15 minutes. NaHB(OAc)3 (170 mg, 0.80 mmol) and AcOH (29 μl, 0.50 mmol) were added and the reaction mixture stirred at room temperature for 1 hour. The reaction mixture was diluted with DCM and washed with sat. NaHCO3 solution followed by brine. The organic extract was dried over anhydrous MgSO4 and filtered. The solvent was removed under reduced pressure. The crude material was purified on a silica column eluting with a solvent gradient of DCM:MeOH:NH3 (100:0:0) gradually changing to (95:5:0.5) to afford the title compound as a colourless oil (75 mg, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214694B2
Source datasetuspto-grants-2007_05
ORD IDord-4b8819e7fb6048cba3a5013cb921557d
Source noteuspto-grants-2007_05