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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289360Generated: October 30, 2026

Acetic Anhydride → HCID 18700154, compound

https://huagongshe.com/reaction/2289360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 18700118HCID 18700118—
SolventDichloromethaneHCID 6344—
ProductHCID 18700154HCID 18700154—

Reaction Steps

To a solution of 1-(1-(2-(2,2,2-trifluoroethoxy)-4-(1-aminocyclohex-4-yl oxy)phenylacetyl)piperidin-4-yl)-4H-3,1-benzoxazin-2(1H)-one hydrochloride (0.090 g, 0.15 mmol) from Example 41 in CH2Cl2 (4 mL) was added acetic anhydride (0.031 mL, 0.3 mmol) and DIEA (0.052 mL, 0.3 mmol). The solution was stirred at ambient temperature for 1 h and the solvent was removed under reduced pressure. The residue was dissolved in EtOAc (50 mL) and washed with 0.25 M aqueous citric acid (20 mL), H2O (10 mL), and saturated aqueous NaHCO3 (20 mL). The organic phase was dried (MgSO4), filtered, and the solvent was removed under reduced pressure to give the title compound as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090805
Source datasetuspto-grants-2000_07
ORD IDord-893ef2121099446fbcd07656c54c4659
Source noteuspto-grants-2000_07