Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995765Generated: October 25, 2026

Carbon Dioxide → 2,4-Diamino-6-(2',4',6'-tribromoanilinomethyl)-1,3,5-triazine

https://huagongshe.com/reaction/1995765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactantethyl N-(2,4,6-tribromophenyl)glycinateHCID 12659467—
ReactantCarbamimidamidomethanimidamideHCID 176517607—
SolventMethanolHCID 887—
Product2,4-Diamino-6-(2',4',6'-tribromoanilinomethyl)-1,3,5-triazineHCID 35308757%

Reaction Steps

Freshly prepared biguanide (6.1 g, 0.06 mole) in methanol (700 ml) was placed in a flask equipped with a stirrer and a soda lime trap to exclude CO2. IV (25.0 g, 0.06 mole) was added all at once through a powder funnel. After the solution was stirred for 10 min at room temperature, a white precipitate began to form. After being stirred for 7.5 h, the mixture was allowed to stand overnight. The crystals were filtered and washed with fresh methanol. They were then slurried with water (250 ml), filtered again, and washed with methanol. A crude yield of 21.9 g (81%) was obtained. It was recrystallized by dissolving 21.8 g in 80 ml of hot DMF (125° C.) and then adding 9 ml of water dropwise. When the solution cooled, white crystals separated. A second crop of crystals was obtained from the filtrate. The total recovery was 15.5 g, a yield of 57% based on the theoretical yield of 27.2 g. An analytical sample with mp of 250°-51° C. was obtained by recrystallizing again from hot DMF and finally washing with cold methanol. Anal. calcd. for C10H9Br3N6 : C, 26.52; H, 2.00; Br, 52.93; N, 18.55. Found: C, 26.52; H, 2.02; Br, 52.71; N, 18.59.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04405806
Source datasetuspto-grants-1983_09
ORD IDord-0edc2fb52d3040bb8c6c660bb4719d79
Source noteuspto-grants-1983_09