Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501065Generated: November 1, 2026

1-Hydroxybenzotriazole → HCID 178425177, compound

https://huagongshe.com/reaction/1501065

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 89581392HCID 89581392—
ReactantHCID 178425242HCID 178425242—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 178425177HCID 17842517729.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 4-(1-(4-fluorophenoxy)ethyl)benzoic acid (260 mg, 1 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (382 mg, 2 mmol), N-hydroxybenzotriazole (270 mg, 2 mmol), triethylamine (0.3 mL) and dichloromethane (15 mL) were stirred at 25° C. for half an hour. Then 3-(aminomethyl)-4,6-dimethylpyridin-2-ol (152 mg, 1 mmol) was added. The mixture was stirred at 25° C. for 12 hours. To the mixture, water (20 mL) was added and the mixture was extracted with dichloromethane (30 mL×3). The combined organic phase was dried by sodium sulfate and then filtered. The filtrate was concentrated in vacuo. The residue was purified by column chromatography (silica gel, dichloromethane/methanol=20:1) to give 4-(1-(4-fluorophenoxy)ethyl)-N-((2-hydroxy-4,6-dimethylpyridin-3-yl)methyl)benzamide (Compound I-46) (115 mg, 29%). LRMS (M+H+) m/z: calcd 394.17. found 394. HPLC purity (214 nm): 94%. 1H NMR (300 MHz, d6-DMSO): δ 11.44 (s, 1H), 8.30 (t, J=5.1 Hz, 1H), 7.77 (d, J=8.4 Hz, 2H), 7.41 (d, J=8.4 Hz, 2H), 7.04-6.85 (m, 4H), 5.83 (s, 1H), 5.47 (q, J=6.6 Hz, 1H), 4.26 (d, J=5.1 Hz, 2H), 2.16 (s, 3H), 2.10 (s, 3H), 1.52 (d, J=6.6 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206128B2
Source datasetuspto-grants-2015_12
ORD IDord-dafbd54e13dd46d488e1be27d10ac22b
Source noteuspto-grants-2015_12