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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789777Generated: November 4, 2026

Water → HCID 11955792, compound

https://huagongshe.com/reaction/1789777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-AminobenzimidazoleHCID 13624—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-4,6-bis(morpholin-4-yl)-1,3,5-triazineHCID 224967—
SolventDimethylformamideHCID 6228—
ProductHCID 11955792HCID 1195579293%

Reaction Steps

9.32 g (70 mmol) of 2-aminobenzimidazole dissolved in DMF (300 ml) was added and reacted with 60% sodium hydride (2.80 g, 70 mmol) at room temperature for 30 minutes. This suspension was added to a solution of 14.3 g (50 mmol) of 2-chloro-4,6-dimorpholino-1,3,5-triazine dissolved in DMF (200 ml) and stirred at room temperature for 2 hours. The reaction solution was poured into water and the resulting precipitates were washed with water and methanol to obtain 17.7 g (yield: 93%) of 2-(2-aminobenz-imidazol-1-yl)-4,6-dimorpholino-1,3,5-triazine. (2) 0.38 g (1.0 mmol) of 2-(2-aminobenzimidazol-1-yl)-4,6-dimorpholino-1,3,5-triazine and 0.24 g (4.0 mmol) of acetic acid were added to and further 0.83 g (4.0 mmol) of DCC was added to chloroform (5 ml) and stirred at room temperature for 4 hours. The reaction solution was poured into water and extracted with ethyl acetate. The separated organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography to obtain 0.31 g (yield: 73%) of the titled compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071189B2
Source datasetuspto-grants-2006_07
ORD IDord-ea4fa84f58b14006b5a9e9d83c326429
Source noteuspto-grants-2006_07