HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-N-Boc-Amino-Thiazole-5-Carboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-((tert-butoxy(hydroxy)methylidene)amino)-1,3-thiazole-5-carboxylate | HCID 7213140 | — |
| Solvent | Tetrahydrofurfuryl alcohol | HCID 7360 | — |
| Product | 2-N-Boc-Amino-Thiazole-5-Carboxylic Acid | HCID 22271442 | — |
Reaction Steps
The second step involves treating a stirred solution of ethyl 2-[(tert-butoxycarbonyl)amino]-1,3-thiazole-5-carboxylate in tetrahydrofuran-methanol with 6N aqueous sodium hydroxide solution at room temperature for 24 hours. Most of the tetrahydrofuran-methanol were removed by distillation under reduced pressure and the aqueous solution was acidified with 6N hydrochloric acid to obtain a solid which was filtered, washed with water and ether, then air dried, followed by drying in vacuo to obtain 2-[(tert-butoxycarbonyl)amino]-1,3-thiazole-5-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365526B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-1239c6fb975d4b24b562a0bf7be81750 |
| Source note | uspto-grants-2016_06 |