HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401502Generated: October 30, 2026
2-(Dimethylamino)ethanol → HCID 57690626, compound
https://huagongshe.com/reaction/401502
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Dimethylamino)ethanol | HCID 7902 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | 2-Fluoro-N-methoxy-N-methylnicotinamide | HCID 53417067 | — |
| Reactant | tert-Butyl 4-(isoquinolin-3-yl)piperazine-1-carboxylate | HCID 57690803 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57690626 | HCID 57690626 | 8% |
Reaction Steps
A solution of 2-dimethylaminoethanol (0.072 ml, 0.72 mmol) in hexanes (3 ml) was cooled down to −40° C. A 2.5M solution of nbutyl lithium in tetrahydrofuran (0.574 ml, 1.44 mmol) was added dropwise. The solution was stirred for 20 minutes. A suspension of tert-butyl 4-(isoquinolin-3-yl)piperazine-1-carboxylate (0.75 mg, 0.24 mmol) in hexanes (8 ml) was added and the resulting solution was stirred for 1 hour. The solution was cooled down to −78° C. A solution of 2-fluoro-N-methoxy-N-methylnicotinamide (176.3 mg, 0.96 mmol) in THF (40 ml) was added dropwise. The reaction mixture was warmed up to −50° and stirred for 1 hour, then the mixture was stirred at 0° C. for a further 1 hour. The crude mixture was partitioned between water and ethyl acetate. The organic extract was dried over magnesium sulfate, filtered and concentrated under vacuo. The residue was and purified on silica gel by flash column chromatography to give the title compound as a yellow oil (8 mg, 8% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741931B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-c1d12809e815467b9afc7a8a7d9b42db |
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| Source note | uspto-grants-2014_06 |
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