HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → Acetic acid 1-ethylcarbamoyl-7-oxiranylmethyl-1H-indazol-6-yl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Acetic Acid 7-allyl-1-ethylcarbamoyl-1H-indazol-6-yl ester | HCID 69564705 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Acetic acid 1-ethylcarbamoyl-7-oxiranylmethyl-1H-indazol-6-yl ester | HCID 86759647 | — |
Reaction Steps
To a solution of the product from Step D (2.70 g, 9.4 mmol) in dichloromethane (15 mL) was added 3-chloro-perbenzoic acid (2.31 g, 10.3 mmol, 77% pure) and the mixture stirred at ambient temperature for 1 h. Additional 3-chloro-perbenzoic (0.2 g, 0.9 mmol) was added and the reaction continued for 3 h. The reaction was quenched with saturated aqueous sodium bicarbonate (100 mL) and extracted with dichloromethane (50 mL). The extract was dried (MgSO4) and evaporated to a white solid (1.59 g, 56%): mp 110-111° C.; LC/MS (+APCI) m/z 304 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06881749B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-98f4503d5c8247e6ac872ab2cd117c55 |
| Source note | uspto-grants-2005_04 |