Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171055Generated: November 2, 2026

Water → HCID 178453011, compound

https://huagongshe.com/reaction/1171055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
Reactant2,2-Difluoro-2-pyridin-2-ylethaneamineHCID 9964167—
Reactant3-Cyano-6-chloro-2-[3-(tert-butoxycarbonyl)amino-benzo[d]isoxazol-6-ylmethyl]aminocarbonylmethyl-pyridine 1-oxideHCID 58972995—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 178453011HCID 178453011—

Reaction Steps

A mixture of 3-cyano-6-chloro-2-[3-(tert-butoxycarbonyl)amino-benzo[d]isoxazol-6-ylmethyl]aminocarbonylmethyl-pyridine 1-oxide (29 mg) and 2,2-difluoro-2-pyridin-2-yl-ethylamine (20 mg) (Organic Process Research & Development 8:192-200, 2004), in DMSO (0.5 mL) was heated overnight at 80° C. LC/MS (ESI) indicated the mono-Boc product (M+H+ 580.1) as the major component. To the reaction vial was added DCM (10 mL) and water (3 mL). The mixture was vigorously stirred. After removing the aqueous layer, the organic layer was further washed with water (4×3 mL) to remove DMSO and water soluble components. Rotary evaporation of solvent afforded a syrupy residue that was used without purification. LCAMS (ESI) showed the mono-Boc product (M+H+ 580.1) as the major component and the di-Boc product (M+H+ 680.0) as a minor component.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829584B2
Source datasetuspto-grants-2010_11
ORD IDord-89d5d2acffb040948bf6a42a327d8fa4
Source noteuspto-grants-2010_11