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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863670Generated: October 30, 2026

Hydrochloric Acid → Bisindolylmaleimide XI hydrochloride

https://huagongshe.com/reaction/863670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylamineHCID 674—
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant3-[8-(Acetoxymethyl)-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl]-4-(1-methyl-3-indolyl)furan-2,5-dioneHCID 10389882—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductBisindolylmaleimide XI hydrochlorideHCID 11605551—

Reaction Steps

185 mg of trifluoromethanesulfonic anhydride in 30 ml of dichloromethane were treated at 0° C. under a nitrogen atmosphere with a suspension of 140 mg of the pyrroledione product of Example 1 and 70 mg of collidine in 25 ml of dichloromethane. After 1.5 hour, 0.8 ml of a 33% solution of dimethylamine in ethanol was added and the mixture was stirred for 2.5 hours. The solvent was removed under reduced pressure and the residue was triturated with methanol to give a solid which was stirred with ethyl acetate saturated with hydrogen chloride. The solid was filtered off and dried to give 70 mg of 3-[6,7,8,9-tetrahydro-8-[(dimethylamino)methyl]pyrido[1,2-a]indol-10-yl]-4-(1-methyl-3-indolyl)-1H-pyrrole-2,5-dione hydrochloride of melting point 335°-336° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05721245
Source datasetuspto-grants-1998_02
ORD IDord-b83a4150614b49c2b63fd84dfa1d1110
Source noteuspto-grants-1998_02