HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881981Generated: October 28, 2026
2-(Methylamino)ethanol → HCID 59331449, compound
https://huagongshe.com/reaction/1881981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Methylamino)ethanol | HCID 8016 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 6-(5-{1-[4-(cyclopropylsulfonyl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)pyridine-3-carbaldehyde | HCID 59331419 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59331449 | HCID 59331449 | 80% |
Reaction Steps
To a solution of 6-(5-{1-[4-(cyclopropylsulfonyl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)pyridine-3-carbaldehyde (200 mg) in 1,2-dichloroethane (5 mL) was added 2-(methylamino)ethanol (80 μL), and the mixture was stirred at room temperature for 30 min. To the reaction mixture was added sodium triacetoxyborohydride (280 mg), and the mixture was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate and saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and the title compound (181 mg, yield 80%) was obtained as a colorless amorphous solid from a fraction eluted with ethyl acetate. MS: 524 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318746B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-c2960db1571d4c98bd3bdc8e7a577391 |
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| Source note | uspto-grants-2012_11 |
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