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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976495Generated: October 31, 2026

Benzoyl chloride → Tert-butyl 1-benzoyl-4-{[4-(2-butynyloxy)phenyl]sulfonyl}-1,4-diazepane-5-carboxylate

https://huagongshe.com/reaction/1976495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
Reactanttert-Butyl 4-{[4-(2-butynyloxy)phenyl]sulfonyl)-1,4-diazepane-5-carboxylateHCID 22644870—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 1-benzoyl-4-{[4-(2-butynyloxy)phenyl]sulfonyl}-1,4-diazepane-5-carboxylateHCID 22644961—

Reaction Steps

tert-Butyl 4-{[4-(2-butynyloxy)phenyl]sulfonyl)-1,4-diazepane-5-carboxylate (0.425 g, 0.96 mmol) in dichloromethane at 25° C. (10 mL) was treated with triethylamine (0.28 mL, 2.02 mmol) followed by benzoyl chloride (0.12 mL, 1.06 mmol) and dimethylaminopyridine (10 mg). After 18 hours aqueous workup gave tert-butyl 1-benzoyl-4-{[4-(2-butynyloxy)phenyl]sulfonyl}-1,4-diazepane-5-carboxylate. 1H NMR (dmso-d6, 300 MH): 1.24 (s, 9H, t-bu), 1.82(s, 3H, CH3 ), 2.0-4.0 (m, 81, CH2 ), 4.65 (s, 1H, CM, 4.85 (s. 21H, CH2 ), 7.0-7.9 (m, 9H, ArH). Treatment with trifluoroacetic acid (4 mL) in dichoromethane (10 mL) for 6hours gave, after concentration in vacuo followed by chromatography on silica gel eluting with dichloromethane/methanol, 1-benzoyl4-{[4-(2-butynyloxy)phenyl]sulfonyl}-1,4-diazepane-5-carboxylic acid as a foam (0.328 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225311B1
Source datasetuspto-grants-2001_05
ORD IDord-c81193d2d8b84ff1ac20749245448f0d
Source noteuspto-grants-2001_05