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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381547Generated: November 1, 2026

HCID 12803100, compound → HCID 12803105, compound

https://huagongshe.com/reaction/1381547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12803100HCID 12803100—
ReactantHCID 178418250HCID 178418250—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 12803105HCID 1280310553%

Reaction Steps

To a solution of 21.3 g (0.124 mole) of 5-aminoindole-3-acetonitrile in 400 ml of 25% aq HOAc cooled to 0° was added 10.5 g (0.13 mole) of KOCN in 30 ml of H2O. The reaction mixture was stored at 0° for 14 hours after which a beige solid was filtered and recrystallized from methanol to give 14.0 g (53% yield) of N-(3-cyanomethyl-1H-indol-5-yl)urea. Further recrystallization affords an analytical sample: m.p. 219°-220°; i.r. (Nujol) 3455, 3300, 2250 and 1650 cm-1 ; nmr (d6 -DMSO) δ(TMS) 11.06 (1,S,indole NH ), 8.46 (1,S, --NHCO--), 7.70 (1,d,Jmeta =2 Hz), 7.37 (1,d,Jortho =9 Hz), 7.30 (1,S,indole C2H), 7.18 (1,d of d,Jortho =9 Hz, Jmeta =2 Hz), 5.73 (2,S,--CONH2) and 4.00 ppm (2,S,--CH2CN).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04803218
Source datasetuspto-grants-1989_02
ORD IDord-974bcd878e9f493098d09e889e2f6392
Source noteuspto-grants-1989_02