Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061629Generated: November 1, 2026

Hydrochloric Acid → HCID 178457304, compound

https://huagongshe.com/reaction/2061629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzofuran-2-carboxylic acidHCID 10331—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178453921HCID 178453921—
SolventTetrahydrofuranHCID 8028—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178457304HCID 17845730463%

Reaction Steps

4.0 M HCl solution in dioxane (1.0 mL, 4.0 mmol) was added to a solution of compound 20 (87 mg, 0.2 mmol) in dioxane (10 mL) and the reaction mixture was stirred at room temperature for 2 hours. Solvent was evaporated in vacuo and the residue was used directly for the next step without further purification. To a solution of the residue in tetrahydrofuran (THF) (20 mL), were added benzofuran-2-carboxylic acid (32 mg, 0.2 mmol), 1-ethyl-3(3-dimethylaminopropyl)carbodiimide (EDCI) (38 mg, 0.2 mmol), 1-hydroxybenzotriazole (HOBT) (27 mg, 0.2 mmol), and diisopropylethylamine (DIPEA) (103 mg, 0.8 mmol). The reaction mixture was stirred at room temperature for 2 hours. Solvent was evaporated in vacuo. The residue was partitioned between ethyl acetate and water. The organic layer was separated and washed with brine, and dried over anhydrous Na2SO4. Flash column chromatography (MeOH/EtOAc, 1:6) gave compound 11 as a colorless oil (60 mg, 63%). 1H NMR (CDCl3, 300 MHz) δ 7.68 (d, 7.6 Hz, 1H), 7.52-7.28 (m, 4H), 6.49 (d, J=8.2 Hz, 1H), 4.82 (s, broad, 2H), 3.98-3.85 (m, 1H), 3.50-2.25 (m, 8H), 2.20-1.10 (m, 16H), 0.94 (t, J=6.6 Hz, 3H); 13C NMR (CDCl3, 75 MHz) δ 158.50, 155.06, 149.22, 128.06, 127.22, 124.08, 123.11, 112.08, 110.71, 52.80, 48.68, 35.63, 33.04, 31.74, 19.26, 11.97, 11.77; HRMS-Electrospray (m/z): [M+H]+ calcd 481.2637. found 481.2637; purity HPLC 99.2%, tR=29.761 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283368B2
Source datasetuspto-grants-2012_10
ORD IDord-ba9d7f5403594606a55345544ac564f2
Source noteuspto-grants-2012_10