Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988767Generated: October 26, 2026

2-Furancarbonyl chloride → Furan-2-carboxylic acid N-(1-Boc-piperidin-3-ylmethyl)-N-phenyl amide

https://huagongshe.com/reaction/988767

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furancarbonyl chlorideHCID 68242—
ReactantN-(1-Boc-piperidin-3-ylmethyl)anilineHCID 12972131—
SolventDichloromethaneHCID 6344—
ProductFuran-2-carboxylic acid N-(1-Boc-piperidin-3-ylmethyl)-N-phenyl amideHCID 5397198493%

Reaction Steps

To a stirred suspension of N-(1-Boc-piperidin-3-ylmethyl)-aniline 4 (61.0 mg, 0.21 mmol) and piperidinomethyl polystyrene resin (60 mg) in 0.6 mL of dry CH2Cl2 was added 2-furoyl chloride (95%, 35.1 mg, 1.2 eq.) at room temperature. After being shaken at room temperature for 4 hours, the reaction mixture was passed through an aminopropyl NH2 cartridge and washed with CH2Cl2. Removal of CH2Cl2 afforded furan-2-carboxylic acid N-(1-Boc-piperidin-3-ylmethyl)-N-phenyl amide 13 (75 mg, 93%). LRMS 285 (M-100)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06635661B2
Source datasetuspto-grants-2003_10
ORD IDord-1f7a7b602bc14806b050a1c361c49b3b
Source noteuspto-grants-2003_10