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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229341Generated: October 30, 2026

Ozone → HCID 11358871, compound

https://huagongshe.com/reaction/2229341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 18466629HCID 18466629—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 11358871HCID 1135887158%

Reaction Steps

A stream of O3 was introduced into a cold (−78° C.) solution of 5,11-dihydro-2,5-dimethyl-11-ethyl-8-(2-propenyl)-6H-dipyrido[3,2-b:2′,3′-e][1,4]diazepin-6-one (187 mg, 0.6 mmol) and Sudan III in CH2Cl2 (3 mL) and MeOH (3 mL). When the pink solution turned brown, O2 was bubbled through the solution for 10 min. NaBH4 (57 mg, 1.52 mmol) was then added and the solution was allowed to warm to room temperature. After 30 min, an additional amount of NaBH4 (20 mg) was added. After 2 h, aqueous saturated NH4Cl was then added and the mixture stirred for 20 min. The solution was concentrated if under reduced pressure and extracted with CH2Cl2 (3×). The combined organic extracts were washed with brine, dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (EtOAc:Hexane 6:4) to give the title compound (111 mg, 58% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420359B1
Source datasetuspto-grants-2002_07
ORD IDord-8dfe1e0110e7460685b073b6a0031b72
Source noteuspto-grants-2002_07