Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456485Generated: October 30, 2026

Acetyl chloride → HCID 67071063, compound

https://huagongshe.com/reaction/1456485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantFumaric AcidHCID 444972—
Reactant2-(4-(6-Fluorobenzo[d]isoxazol-3-yl)piperidin-1-yl)ethan-1-amineHCID 14699857—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 67071063HCID 67071063—

Reaction Steps

A a mixture of 2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethylamine (2.56 g, 9.7 mmol) and triethylamine (1.45 g, 14.5 mmol) in DCM (50 ml) was treated with dropwise addition of acetyl chloride (1.0 g, 12.7 mmol) at room temperature. The mixture was stirred for 4 hours at room temperature. The reaction mixture was diluted with DCM and washed with brine. The organic solution was dried over MgSO4 and concentrated to a crude oil. The crude oil was purified by flash chromatography over a silica gel column (SiO2, 20 g; eluted with (0-2%) CH3OH in DCM). The pure product thus obtained weighed 1.36 g (46%). It was converted to a fumarate salt by treatment with fumaric acid (517 mg) in ethanol. Recrystallization from ethanol gave white crystals; weight: 1.53 g, m.p.=132°-133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843949
Source datasetuspto-grants-1998_12
ORD IDord-01af49069ea845afae70bbd25c3d15fb
Source noteuspto-grants-1998_12