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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715071Generated: October 30, 2026

Benzoyl chloride → HCID 58840909, compound

https://huagongshe.com/reaction/1715071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantHCID 58840911HCID 58840911—
SolventAcetonitrileHCID 6342—
ProductHCID 58840909HCID 5884090978.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring solution of (7S)-7-amino-7-(quinolin-6-ylcarbamoyl)-heptanoic acid tert-butyl ester (8.0 g, 21.6 mmol) in dry MeCN (100 mL) and to this solution was added benzoyl chloride (2.78 mL, 23.8 mmol) and triethylamine (6.1 mL, 43.2 mmol). The solution was stirred at 0° C. for 1 h, then at RT for 2 h. The solvent was removed, and residue was dissolved in 400 mL EtOAc, and stirred with 100 mL 0.5 M NaHCO3 for 1 h. The aqueous layer was removed, and the organic layer was washed with 100 mL 0.5 M NaHCO3, then with 50 mL water. The solution was dried over anhydrous Na2SO4. The product (8.1 g) was obtained after column purification (EtOAc as eluent) in 78.8% yield as a thick oil. 1H NMR (CDCl3) δ 9.40 (1H, s), 8.80 (1H, d), 8.22 (1H, d), 8.0-7.0 (10H, m), 5.0 (1H, m), 2.2-1.2 (19H, m). MS (ESI): (MH+) 476.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799803B2
Source datasetuspto-grants-2010_09
ORD IDord-c8d6198ff90c405f8094085b9a296049
Source noteuspto-grants-2010_09