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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815913Generated: October 29, 2026

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

https://huagongshe.com/reaction/1815913

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 O2C 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 (Step 2) (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 numberUS06881737B2
Source datasetuspto-grants-2005_04
ORD IDord-906c9b8f6b7e40708aefcea9db54448c
Source noteuspto-grants-2005_04