Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791177Generated: October 27, 2026

Water → 1-(4-chloro-[1,3,5]triazin-2-yl)-1H-benzoimidazol-2-ylamine

https://huagongshe.com/reaction/1791177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-AminobenzimidazoleHCID 13624—
Reactant2,4-Dichloro-1,3,5-triazineHCID 17810—
ReactantDiisopropylethylamineHCID 81531—
SolventDimethylformamideHCID 6228—
Product1-(4-chloro-[1,3,5]triazin-2-yl)-1H-benzoimidazol-2-ylamineHCID 2353569183%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 1.0 g (6.67 mmol) of 2,4-dichloro-1,3,5-triazine in 3 mL of DMF at 0° C. is added 1.16 mL (6.67 mmol) of DIEA. The resulting yellow solution is stirred at 0° C. for 10 min when-888 mg (6.67 mmol) of 2-aminobenzimidazole is added portionwise over 5 min, followed by an additional 1 mL of DMF. The resulting mixture is stirred at 0° C. for 1.9 h, then at RT for 3.25 h. At this point, the mixture is poured into 40 mL of stirring cold water with additional cold water rinses to a total volume of 100 mL. The light yellow solid is isolated by filtration, rinsed with cold water, and dried in vacuo, giving 1.36 g (83%) of 1-(4-chloro-[1,3,5]triazin-2-yl)-1H-benzoimidazol-2-ylamine (Compound 1174) as a light yellow solid: MS m/z=246 [M+H]+; HPLC Rt=5.79 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074789B2
Source datasetuspto-grants-2006_07
ORD IDord-312d7d2a6a2543d7a04ff7f6190d2754
Source noteuspto-grants-2006_07