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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989200Generated: October 30, 2026

1,1'-Carbonyldiimidazole → HCID 18005174, compound

https://huagongshe.com/reaction/989200

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant6-Chloro-5-methyl-2,3-dihydro-1H-indoleHCID 22186080—
Reactant264617-04-1HCID 22473585—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 18005174HCID 1800517457%

Reaction Steps

4-Methyl-3-(pyrid-3-yl) aniline (0.30 g, 0.0016 mole) in dry dichloromethane (20 ml) was added, under argon, to 1,1′-carbonyldiimidazole in dry dichloromethane (10 ml) (0.30 g. 0.0018 mole) and stirred at ambient temperature for 1 hour. The solvent was removed in vacuo and the residue dissolved in dry dimethylformamide (30 ml). 6-Chloro-5-methylindoline (see WO 95/01976) (0.27 g, 0.0016 mole) in dry dimethylformamide (10 ml) was added and the mixture heated to 100° C. for 1 hour. After cooling to ambient temperature, the solvent was removed in vacuo and the residue diluted with deionised water (15 ml), extracted into dichloromethane (2×20 ml), dried (Na2SO4) and evaporated in vacuo. The residue was purified by flash column chromatography on silica gel, eluting with 3% methanol/dichloromethane and the resulting solid recrystallised from ethyl acetate/methanol/60.80° petroleum ether to afford the title compound (0.31 g, 57%) as a cream solid (mp 202-203° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638953B2
Source datasetuspto-grants-2003_10
ORD IDord-7a6ebdaf137f45108ba63e34c7d108a7
Source noteuspto-grants-2003_10