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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522887Generated: October 25, 2026

3-Amino-1-propanol → 3-(4-(3-hydroxypropylamino)-1,3,5-triazin-2-ylamino)-N-methylbenzamide

https://huagongshe.com/reaction/522887

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-1-propanolHCID 9086—
Reactant2,4-Dichloro-1,3,5-triazineHCID 17810—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Amino-N-methylbenzamideHCID 676526—
ReactantChloro-triazineHCID 18318800—
SolventDimethylformamideHCID 6228—
Product3-(4-(3-hydroxypropylamino)-1,3,5-triazin-2-ylamino)-N-methylbenzamideHCID 6737690885.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2,4-dichloro-1,3,5-triazine (0.300 g, 2.000 mmol) in DMF (6670 μL) was added N-ethyl-N-isopropylpropan-2-amine (1048 μL, 6.000 mmol). The reaction vessel was cooled in an ice-water bath prior to the addition of 3-amino-N-methylbenzamide (300 mg, 2.000 mmol). The reaction mixture was stirred for 3 h at 0° C. at which time LC-MS revealed complete conversion to the desired chloro-triazine intermediate. To this yellow solution was added 3-aminopropan-1-ol (150 mg, 2.000 mmol). The reaction mixture was allowed to stir and warm slowly to RT over 18 h. Solids had precipitated out of the solution. The solid was filtered off, washed with water, and very little methanol to obtain 3-(4-(3-hydroxypropylamino)-1,3,5-triazin-2-ylamino)-N-methylbenzamide (516 mg, 1.707 mmol, 85%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334269B2
Source datasetuspto-grants-2016_05
ORD IDord-001d32734168482199a42f5d6c54df26
Source noteuspto-grants-2016_05