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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057048Generated: November 2, 2026

1-Hydroxybenzotriazole → HCID 90015403, compound

https://huagongshe.com/reaction/1057048

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-methyl-1H-imidazole-4-carboxylic acidHCID 541509—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 117953310HCID 117953310—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 90015403HCID 9001540315.3%

Reaction Steps

To a mixture of 1-methylimidazole-4-carboxylic acid (39.79 mg, 0.315 mmol, 1.5 equiv.), HOBT (57.42 mg, 0.420 mmol, 2.0 equiv.), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (81.46 mg; 0.420 mmol, 2.0 equiv.) in chloroform (3.0 mL) was added 6-[(2R)-2-methylpyrrolidin-1-yl]-4-pyrrolidin-3-yl-N-[4-(trifluoromethyl)-2-pyridyl]pyridin-2-amine hydrochloride (90 mg, 0.210 mmol) followed by DIPEA (0.148 mL, 0.841 mmol, 4.0 equiv.). The resulting mixture was stirred at rt for 2 h. It was diluted with DCM (10 mL), washed with 10% citric acid and 1 N NaHCO3, dried over Na2SO4, filtered, concentrated in vacuo, and purified by HPLC to afford 16.1 mg (15.3%) of product as yellow solid. 1H NMR (400 MHz, DMSO) δ 9.74 (s, 1H), 8.80 (s, 1H), 8.41 (d, J=5.1 Hz, 1H), 7.68-7.60 (m, 2H), 7.10 (d, J=5.1 Hz, 1H), 6.39 (s, 1H), 5.90 (s, 1H), 4.48-4.09 (m, 3H), 3.94-3.73 (m, 2H), 3.69 (d, J=5.2 Hz, 3H), 3.56-3.43 (m, 2H), 3.25-3.18 (m, 1H), 2.31-2.13 (m, 1H), 2.12-1.86 (m, 4H), 1.73-1.63 (m, 1H), 1.17 (d, J=6.0 Hz, 3H). LC-MS: m/z=500 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399636B2
Source datasetuspto-grants-2016_07
ORD IDord-1fb1690bc84b42ff8629e573e6bc8f24
Source noteuspto-grants-2016_07