HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588408Generated: October 30, 2026
Diisopropylamine → HCID 67407672, compound
https://huagongshe.com/reaction/588408
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 3-Fluoropyridine | HCID 67794 | — |
| Reactant | 3-Furancarboxamide,tetrahydro-N-methoxy-N-methyl-(9CI) | HCID 45084522 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67407672 | HCID 67407672 | 10% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09227967B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-f9ef90aad4c8444488d428b636413557 |
|---|
| Source note | uspto-grants-2016_01 |
|---|