HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113724Generated: November 2, 2026
Dimethylformamide dimethyl acetal → (2E)-1-(1,3-diethyl-1H-indazol-6-yl)-3-(dimethylamino)prop-2-en-1-one
https://huagongshe.com/reaction/2113724
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | 1-(1,3-Diethyl-1H-indazol-6-yl)-ethanone | HCID 59810837 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2E)-1-(1,3-diethyl-1H-indazol-6-yl)-3-(dimethylamino)prop-2-en-1-one | HCID 59810785 | 1.7% |
Reaction Steps
1,1-dimethoxy-N,N-dimethylmethanamine (0.891 g, 0.0075 mol) was added to a solution of 1-(1,3-Diethyl-1H-indazol-6-yl)-ethanone (0.187 mg, 8.64 mmol) in N,N-dimethylformamide (8 mL), and the resulting mixture was shaken at 120° C. for 16 hours. 1,1-dimethoxy-N,N-dimethylmethanamine (0.618 g, 0.0052 mol) was added, and the reaction was refluxed at 140° C. for a further 16 hours. The solvent was removed in vacuo, and the residue extracted with ethyl acetate (30 mL) and water (10 mL). The aqueous layer was re-extracted with ethyl acetate (30 mL). The organic layers were combined, dried, filtered and concentrated. The resulting crude product was purified by silica-gel chromatography, using an eluent gradient of 0.25-0.5% methanol in dichloromethane (mobile phase contained 0.5% ammonium hydroxide solution) to afford 35 mg of (2E)-1-(1,3-diethyl-1H-indazol-6-yl)-3-(dimethylamino)prop-2-en-1-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432266B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-ccf570d6cb094a188b0120fec17a0504 |
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| Source note | uspto-grants-2008_10 |
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