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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170145Generated: October 30, 2026

Benzylamine → N-benzyl-2-chloro-5-phenylpyrrolo[2,1-f][1,2,4]triazin-4-amine

https://huagongshe.com/reaction/2170145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 90386287HCID 90386287—
SolventTetrahydrofuranHCID 8028—
ProductN-benzyl-2-chloro-5-phenylpyrrolo[2,1-f][1,2,4]triazin-4-amineHCID 9038607663.2%

Reaction Steps

2,4-Dichloro-5-phenylpyrrolo[2,1-f][1,2,4]triazine (0.500 g, 1.89 mmol) was dissolved in THF (10 mL) then was added DIPEA (1.65 mL, 9.47 mmol), followed by benzylamine (0.406 g, 3.79 mmol). Then the reaction mixture was stirred at room temperature for 2 h. The reaction mixture was concentrated under reduced pressure to remove THF. To this residue, water (10 mL) was added and the aqueous solution was extracted with CH2Cl2 (25×3 mL). The organic layer was separated and dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography using CombiFlash (REDISEP®, silica gel, 24 g, 11% EtOAc/hexanes) to afford N-benzyl-2-chloro-5-phenylpyrrolo[2,1-f][1,2,4]triazin-4-amine (0.400 g, 63.1%). LCMS Condition B-47: retention time 2.70 min, [M+1]=335.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09050345B2
Source datasetuspto-grants-2015_06
ORD IDord-cd009d28f3c143a9b816ffa6612975b6
Source noteuspto-grants-2015_06