Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395706Generated: October 26, 2026

K-252C → Ngic-I

https://huagongshe.com/reaction/2395706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantK-252CHCID 3815—
ReactantAcetonitrileHCID 6342—
ReactantUndec-4-eneHCID 136496—
ProductNgic-IHCID 3714—

Reaction Conditions

Temperature20 °C

Reaction Steps

300 mg (0.96 mmole) 6,7,12,13-tetrahydro-5-oxo-5H-indolo[2.3-a]pyrrolo [3,4-c]carbazole, suspended in 20 mL acetonitrile, are mixed with 0.3 mL (4.56 mole) acrylic acid nitrile and 2 drops of 1,8-diazabicyclo[5,4,0[undec-7-ene (DBU) and stirred for 3 days at 20° C. The mixture of starting materials and product is filtered off, again mixed with the same amounts of acrylic acid nitrile, DBU and acetonitrile and stirred for a further 3 days at 20° C. After again repeating this procedure and after a further 3 days at 20° C., the 12-(2-cyanoethyl)-6,7,12, 13-tetrahydro-5-oxo-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole is filtered off in the form of beige colored crystals which decompose above 275° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05489608
Source datasetuspto-grants-1996_02
ORD IDord-88f9310c8bde4528a8005ced7eac3c75
Source noteuspto-grants-1996_02