HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559799Generated: October 30, 2026
N-Methylacetamide → HCID 66725500, compound
https://huagongshe.com/reaction/559799
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylacetamide | HCID 6582 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 66725214 | HCID 66725214 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 66725500 | HCID 66725500 | 47% |
Reaction Steps
A solution of POCl3 (0.030 g, 0.2 mmol) in CHCl3 (1 ml) and pyridine (1 ml) was added to N-methylacetamide (0.015 g, 0.2 mmol) and the mixture was cooled in an ice-water bath and stirred for 90 minutes. To this solution was added a solution of 5-hydrazinocarbonyl-6-methyl-2-oxo-1-(3-trifluoromethyl-phenyl)-1,2-dihydro-pyridine-3-carboxylic acid 4-methanesulfonyl-benzylamide (Example 38 (a), 0.040 g, 0.076 mmol) in CHCl3 (2 ml) and the mixture was stirred overnight at room temperature. Purification by preparative HPLC gave the linear intermediate (0.020 g). This material was suspended in EtOAc (2 ml) and was heated (90° C.) with stirring for 4 h, giving rise to a mixture of three components. This mixture was purified on preparative HPLC giving the title compound (0.003 g, 7%) after freeze-drying the pure fractions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063073B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-03ca21c56b004ceb8fabaee68886591c |
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| Source note | uspto-grants-2011_11 |
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