Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Amino-3-chloro-6-methylbenzamide | HCID 23446879 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 23446892 | HCID 23446892 | — |
Reaction Steps
1.18 g (0.033 mol) of hydrogen chloride, dissolved in 35 ml of diethyl ether, were added at 22 to 30° C. with stirring to a suspension of 5 g (0.027 mol) of the compound from example 3 in 50 ml of 1,2-dichloroethane and the mixture was then concentrated in vacuo. The residue was treated with 150 ml of phosphorus oxychloride and the mixture was stirred at 120° C. for 3 h. The reaction mixture was then concentrated in vacuo, the residue was dissolved in methylene chloride, and the solution was treated with water and neutralized using 2 N sodium hydroxide solution. After the phase separation, the organic phase was again washed with water, then with saturated sodium chloride solution, and dried over magnesium sulfate. After concentration, 2.4 g (48% of theory) of the title compound were obtained as a yellowish powder of m.p. 77-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06683213B1 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-8479d47b6bc3457cbc42a520fb41b705 |
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| Source note | uspto-grants-2004_01 |
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