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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476661Generated: October 31, 2026

(6,8a-Dimethoxy-1,5-dimethyl-4,7-dioxo-1,1a,2,4,7,8,8a,8b-octahydroazireno[2',3':3,4]pyrrolo[1,2-a]indol-8-yl)methyl hydrogen carbonimidate → HCID 88629345, compound

https://huagongshe.com/reaction/476661

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6,8a-Dimethoxy-1,5-dimethyl-4,7-dioxo-1,1a,2,4,7,8,8a,8b-octahydroazireno[2',3':3,4]pyrrolo[1,2-a]indol-8-yl)methyl hydrogen carbonimidateHCID 159845—
ReactantSodium AcetateHCID 517045—
Reactant2-Chloroethylamine hydrochlorideHCID 9793737—
SolventMethanolHCID 887—
ProductHCID 88629345HCID 8862934582.9%

Reaction Steps

To a solution of 33 mg (0.09 mmol) of N-methylmitomycin A in 5 ml of anhydrous methanol, a solution of 56 mg of 2-chloroethylamine hydrochloride (0.5 mmol) in 2.5 ml of methanol and a solution of 41 mg sodium acetate (0.5 mmol) in 2.5 ml of methanol were added alternatively with constant stirring over a period of 10 minutes. The stirred reaction mixture was checked frequently by TLC and the reaction appeared to be complete in 24 hours. The solvent was evaporated and the residue was chromatographed using silica-gel as adsorbent. The fraction obtained by eluting the column with ethyl acetate was evaporated under reduced pressure. Recrystallization from a mixture of chloroform and hexane gave 16 mg (38% yield) of the desired product as purple-colored crystals having a melting point of 73°-74° C. (decomposing) and providing the following analysis:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04885304
Source datasetuspto-grants-1989_12
ORD IDord-ee48d41e82f6475089fc72ebb77b58e9
Source noteuspto-grants-1989_12