HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621906Generated: October 31, 2026
1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamine → HCID 14390471, compound
https://huagongshe.com/reaction/621906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamine | HCID 547712 | — |
| Reactant | HCID 15617180 | HCID 15617180 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 14390471 | HCID 14390471 | 45.1% |
Reaction Steps
Under a nitrogen atmosphere, N,N-dimethylformamide-ditert-butyl acetal (8.12 g, 0.040 mole) was added dropwise over a 20-minute period to a stirred, refluxing suspension of 2-(2-pyridyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (2.54 g, 0.010 mole) in anhydrous benzene (50 ml). The resulting solution was refluxed for 1 hour and allowed to cool to room temperature. The reaction mixture was washed with 10% potassium carbonate solution (2×25 ml), water (25 ml), dried over sodium sulfate and concentrated in vacuo. The residue (3.5 g) was dissolved in tetrahydrofuran and treated with excess ethereal hydrogen chloride. The crystalline solid was recrystallized from tetrahydrofuran, giving 1.5 g (43%). Drying in vacuo at 65° C. for 8 hours and then at 78° C. overnight gave 1.4 g of the compound as the free base, mp 124°-125.5°0 C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04824951 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-e0ff8ff59688400ea91f497f9e781b8d |
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| Source note | uspto-grants-1989_04 |
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