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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588408Generated: October 30, 2026

Diisopropylamine → HCID 67407672, compound

https://huagongshe.com/reaction/588408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant3-FluoropyridineHCID 67794—
Reactant3-Furancarboxamide,tetrahydro-N-methoxy-N-methyl-(9CI)HCID 45084522—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67407672HCID 6740767210%

Reaction Steps

Diisopropylamine (605 μL, 4.30 mmol) was dissolved in THF (8 mL) and cooled to −78° C. nBuLi (1.72 mL, 2.5 M in hexanes, 4.30 mmol) was added and the resulting solution was stirred for 10 min, warmed to room temperature for 30 min and re-cooled to −78° C. 3-Fluoro-pyridine (370 μL, 4.30 mmol) was added drop-wise and the reaction mixture was stirred for 2 h. A solution of N-methoxy-N-methyloxolane-3-carboxamide (685 mg, 4.30 mmol) in THF (4.2 mL) was added drop-wise and the reaction mixture was warmed to room temperature and stirred for 15 min. The reaction mixture was quenched with sat aq NH4OAc (5 mL), diluted with EtOAc (50 mL), washed with water (2×25 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by normal phase column chromatography to give the title compound as a yellow gum (61.0 mg, 10%). LCMS (ES+): 196.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227967B2
Source datasetuspto-grants-2016_01
ORD IDord-f9ef90aad4c8444488d428b636413557
Source noteuspto-grants-2016_01