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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052891Generated: October 31, 2026

4-Methylmorpholine → HCID 10050252, compound

https://huagongshe.com/reaction/2052891

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant4-Chloro-benzo[e][1,3]oxazin-2-oneHCID 11309887—
ReactantHCID 59654225HCID 59654225—
SolventAcetonitrileHCID 6342—
ProductHCID 10050252HCID 1005025216%

Reaction Steps

A suspension of 4-chloro-benzo[e][1,3]oxazin-2-one (620 mg, 3.41 mmol, 2.0 eq), 2-amino-5,5-dimethyl-heptanoic acid (4-cyano-1-propyl-piperidin-4-yl)-amide (675 mg, 1.71 mmol, 1.00 eq), and 4-methylmorpholine (NMM) (0.56 mL, 5.09 mmol, 3.00 eq) in acetonitrile (9.0 mL) was stirred at room temperature overnight. The reaction mixture was then concentrated, resuspended in ethyl acetate (50 mL) and washed with saturated Na2CO3 solution. The organic phase was dried (MgSO4) and concentrated and the resulting residue was chromatographed over silica gel using a gradient of methanol in dichloromethane as the eluant to provide 124 mg (16% yield) of the title compound; m/z calculated for C26H37N5O3 467.6, found 468.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326719B2
Source datasetuspto-grants-2008_02
ORD IDord-83082695e2ff43f49cbd2110fac3e754
Source noteuspto-grants-2008_02