HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245404Generated: October 28, 2026
N-Methoxy-N-methylacetamide → methyl 5-acetyl-3-chloro-2-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-4-fluorobenzoate
https://huagongshe.com/reaction/245404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methoxy-N-methylacetamide | HCID 537505 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | methyl 3-chloro-2-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-4-fluorobenzoate | HCID 67358498 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl 5-acetyl-3-chloro-2-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-4-fluorobenzoate | HCID 86658064 | — |
Reaction Steps
To a stirred solution of LDA (3.1 eq) at −50° C. in THF was added methyl 3-chloro-2-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-4-fluorobenzoate (Intermediate 47, 1.5 g, 4.96 mmol) in anhydrous THF (10 mL) dropwise and the solution was stirred for 1 h at −50° C. N-methoxy-N-methylacetamide (1.66 g, 14.9 mmol) in THF (5 mL) was added dropwise and stirring was continued for additional 1 h. The reaction mixture was quenched with saturated aqueous ammonium chloride and extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous sodium sulphate. The solvent was removed under vacuum and the residue was purified over silica gel chromatography column using ethyl acetate-pet. ether gradient to obtain the title compound. Yield: 800 mg, (47%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658641B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-0ff46622f7314ddeb952c8d535fefb70 |
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| Source note | uspto-grants-2014_02 |
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