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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289358Generated: October 30, 2026

Acetic Anhydride → HCID 18700090, compound

https://huagongshe.com/reaction/2289358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 18700134HCID 18700134—
SolventDichloromethaneHCID 6344—
ProductHCID 18700090HCID 18700090—

Reaction Steps

To a solution of 1-(1-(4-(4-piperidinyloxy)-2-(trifluoromethoxy)-phenylacetyl)piperidin-4-yl)-4H-3,1-benzoxazin-2(1H)-one hydrochloride (0.45 g, 0.77 mmol) from Example 39 in CH2Cl2 (50 mL) was added acetic anhydride (0.15 mL, 1.5 mmol) and DIEA (0.26 mL, 1.5 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 (100 mL) and washed with 0.25 M aqueous citric acid (50 mL), H2O (25 mL), and saturated aqueous NaHCO3 (75 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-5ae2b967a8444d4cb7cd6b2f77bf54a4
Source noteuspto-grants-2000_07