HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200339Generated: October 30, 2026
Ethyl Acetate → methyl 3-chloro-7-(2,2-dimethylpropionylamino)-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate
https://huagongshe.com/reaction/2200339
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178498846 | HCID 178498846 | — |
| Product | methyl 3-chloro-7-(2,2-dimethylpropionylamino)-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate | HCID 89705413 | — |
Reaction Steps
A suspension of methyl 7-(2,2-dimethylpropionylamino)-3-hydroxy-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate (Intermediate 9, 1.12 g) in phosphoryl chloride (10 mL) was stirred and heated at 95° C. for 45 minutes. After cooling, the mixture was poured into a mixture of ice and ethyl acetate. The organic phase was washed with water and sodium bicarbonate solution, dried (Na2SO4) and filtered. The filtrate was evaporated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-15% to give methyl 3-chloro-7-(2,2-dimethylpropionylamino)-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate (1.02 g) as a light coloured solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359369B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-ed7b0698cae0467a997d4f9a110ad052 |
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| Source note | uspto-grants-2016_06 |
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