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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170171Generated: October 30, 2026

Water → 4-(Benzylamino)-5-phenylpyrrolo[2,1-f][1,2,4]triazine-2-carboxylic acid

https://huagongshe.com/reaction/2170171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-ButanolHCID 6386—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-(Benzylamino)-5-phenylpyrrolo[2,1-f][1,2,4]triazine-2-carbonitrileHCID 90386190—
Product4-(Benzylamino)-5-phenylpyrrolo[2,1-f][1,2,4]triazine-2-carboxylic acidHCID 9038626928.3%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a stirred solution of 4-(benzylamino)-5-phenylpyrrolo[2,1-f][1,2,4]triazine-2-carbonitrile (0.100 g, 0.307 mmol) dissolved in tert-butanol (15.0 mL, 157 mmol) and water (15 mL) was added potassium tert-butoxide (0.138 g, 1.23 mmol). The reaction mixture was heated in a pressure tube to 95° C. for 16 h and concentrated under reduced pressure. To the resulting residue, was added water (100 mL) and the aqueous solution was neutralized with dilute HCl to pH 7. The solid precipitated, was filtered and further purified by preparative HPLC (Condition B-74 as described in general methods) to afford 4-(benzylamino)-5-phenylpyrrolo[2,1-f][1,2,4]triazine-2-carboxylic acid (30.0 mg, 28.3%). LCMS Condition B-15: retention time 1.66 min, [M+1]=345.2. HPLC Condition B-1: retention time 14.64 min, Purity 99.30%. 1H NMR (400 MHz, DMSO-d6) δ ppm 4.71 (s, 2H), 6.29 (br s, 1H), 6.77 (d, J=2.8 Hz, 1H), 7.24-7.48 (m, 10H), 7.77 (d, J=2.8 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09050345B2
Source datasetuspto-grants-2015_06
ORD IDord-4f6d35047d894907b0ce86a129ff3456
Source noteuspto-grants-2015_06