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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107023Generated: October 31, 2026

Methylamine → HCID 18790704, compound

https://huagongshe.com/reaction/1107023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantHCID 9838629HCID 9838629—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 18790704HCID 18790704—

Reaction Steps

A solution of 0.93 g of the ethyl ester of (4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-9-yl)acetic acid, 20 ml of methylamine as a 33% solution in ethanol and 20 ml of methanol under an argon atmosphere is stirred at a temperature in the region of 20° C. for 18 hours. The reaction mixture is filtered. The precipitate obtained is washed successively with three times 40 ml of ethanol and three times 40 ml of methyl-tert-butyl ether and dried under reduced pressure (15 mm Hg; 2 kPa) at 20° C. The solid obtained is suspended in a mixture of acetone (25 ml) and methanol (5 ml) and stirred for 15 minutes and then filtered, washed with 10 ml of acetone and dried under reduced pressure (1 mm Hg; 0.13 kPa) at 60° C. 0.32 g of N-methyl-2-(4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-9-yl) acetamide is obtained in the form of a white solid, the melting point of which is greater than 260° C. (Analysis C16H14N4O2; % Calculated C: 65.30, H: 4.79, N: 19.04; % Found C: 65.00, H: 4.50, N: 18.80).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057454
Source datasetuspto-grants-2000_05
ORD IDord-462cf64f7cb6430a8901f044cda0695a
Source noteuspto-grants-2000_05