HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643063Generated: October 30, 2026
Diisopropylethylamine → HCID 90763427, compound
https://huagongshe.com/reaction/643063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(2-Oxo-1(2H)-pyridyl)-N,N,N',N'-tetramethyluronium Tetrafluoroborate | HCID 2733204 | — |
| Reactant | HCID 70225858 | HCID 70225858 | — |
| Reactant | HCID 86599729 | HCID 86599729 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90763427 | HCID 90763427 | 76% |
Reaction Steps
A solution of Example 7B (0.36 g, 0.77 mmol) in dichloromethane (5 mL) was treated with O-(1,2-dihydro-2-oxo-1-pyridyl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (TPTU) (0.344 g, 1.5 equivalent), and diisopropylethyl amine (0.4 μL, 3 equivalents) at 0° C. over 20 min. A solution of Example 3A (0.22 g, 1.5 equivalent) in dichloromethane (5 mL) was added at 0° C. and the mixture was stirred at 25° C. for 16 hrs. The mixture was washed with water, 10% sodium bicarbonate, brine, the organic layer was separated, dried over sodium sulfate, filtered and the solvents were evaporated. The crude residue was purified using 1% methanol/chloroform to give 0.37 g (76%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696226B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-1a68335bcdf740df943883e539d1c355 |
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| Source note | uspto-grants-2010_04 |
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