HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 5-Thiazolecarboxamide, 2-(2-methoxyphenyl)-4-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethyl 2-chloroacetoacetate | HCID 11858 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | 2-Methoxybenzamide | HCID 75540 | — |
| Reactant | Ethyl 4-Methyl-2-(2-methoxyphenyl)thiazole-5-carboxylate | HCID 13576837 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Thiazolecarboxamide, 2-(2-methoxyphenyl)-4-methyl- | HCID 3068072 | 70% |
Reaction Steps
Into a solvent mixture of 50 ml of aqueous 28% ammonia and 450 ml of ethanol, 13.9 g of ethyl 2-(2-methoxyphenyl)-4-methylthiazole-5-carboxylate which had been prepared by heating a mixture of o-methoxybenzamide, ethyl α-chloroacetoacetate and phosphorus pentasulfide under a reflux condenser for 5 hours was dissolved. Then in a similar manner as in Example 3 the object was obtained as colourless minute aciculate melting at 191° to 192.5° C. in an amount of 8.7 g corresponding to the yield of 70%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04558059 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-0e9fc0c8479b48fab0fa64aa08edf051 |
| Source note | uspto-grants-1985_12 |