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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983425Generated: October 30, 2026

Diethyl Ether → (1-benzyl-1H-indazol-5-yl)-(4-chloro-[1,3,5]triazin-2-yl)amine

https://huagongshe.com/reaction/983425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(Phenylmethyl)-1H-indazol-5-amineHCID 212069—
Reactant2,4-Dichloro-1,2,5-triazineHCID 22028126—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(1-benzyl-1H-indazol-5-yl)-(4-chloro-[1,3,5]triazin-2-yl)amineHCID 22496107—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 2,4-dichloro-1,2,5-triazine (526.1 mg, 3.51 mmol) in DMF (15 mL) at 0° C. was added DIEA (0.733 mL, 4.21 mmol). The resulting yellow solution was stirred at 0° C. for 20 min and 1-benzyl-1H-indazol-5-ylamine (783.5 mg, 3.51 mmol) was added in one portion followed by 2×2.5 mL DMF flask rinses. The resulting mixture was stirred at 0° C. for 30 min, at RT for 4.5 h, then diluted with EtOAc. The organic layer was washed twice with water and once with brine. The aqueous layer and washings were extracted with EtOAc. The combined organics were dried, concentrated, and purified by chromatography (SiO2, elution with 1:1 EtOAc-hexanes) to give a slightly impure pinkish solid. Trituration with Et2O gave (1-benzyl-1H-indazol-5-yl)-(4-chloro-[1,3,5]triazin-2-yl)amine as a light pink solid: MS m/z=337 [M+H]+. Calc'd for C17H13ClN6: 336.09.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864255B2
Source datasetuspto-grants-2005_03
ORD IDord-22ab324bd8624213ae47e47ebc64ac9e
Source noteuspto-grants-2005_03