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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815940Generated: October 31, 2026

m-Chloroperbenzoic acid → Acetic acid 1-ethylcarbamoyl-7-oxiranylmethyl-1H-indazol-6-yl ester

https://huagongshe.com/reaction/1815940

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantAcetic Acid 7-allyl-1-ethylcarbamoyl-1H-indazol-6-yl esterHCID 69564705—
SolventDichloromethaneHCID 6344—
ProductAcetic acid 1-ethylcarbamoyl-7-oxiranylmethyl-1H-indazol-6-yl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881749B2
Source datasetuspto-grants-2005_04
ORD IDord-98f4503d5c8247e6ac872ab2cd117c55
Source noteuspto-grants-2005_04