HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 14541744, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Glycine, N-(2,1,3-benzoxadiazol-5-ylcarbonyl)-, methyl ester | HCID 14541753 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14541744 | HCID 14541744 | — |
Reaction Steps
500 mg (2.13 mmol) [(benzo[1,2,5]oxadiazole-5-carbonyl)-amino]-acetic acid methyl ester are treated in 50 mL methanol with 6 mL (3 eq.) 1N KOH in methanol containing 10% water at room temperature for two hours, then cooled below 5° C. and neutralized with 6 mL 1 N aqueous HCl. The reaction mixture is extracted with ethyl acetate, the combined organic phases are washed with brine and dried with sodium sulfate, then evaporated to dryness to yield the desired product as a beige-pinkish powder. MS (ES−): 220 (M−1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07632851B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-be20d1aa8377449e8e60be24b14b604a |
| Source note | uspto-grants-2009_12 |