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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174554Generated: November 3, 2026

Hydrochloric Acid → HCID 58074318, compound

https://huagongshe.com/reaction/1174554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant1-(2-Chlorophenyl)ethanolHCID 26082—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 50990322HCID 50990322—
SolventDichloromethaneHCID 6344—
ProductHCID 58074318HCID 5807431833%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(2-Chloro-phenyl)-ethanol (1.0 g, 6.39 mmol, 3.6 Eq) and Et3N (1.16 mL, 8.30 mmol, 4.7 Eq) were dissolved in anhydrous DCM (20 mL) and cooled to 0° C. under nitrogen. MsCl (645 μL, 8.30 mmol, 4.7 Eq) was added portionwise. After 3.5 hours, the reaction was poured into 1M HCl (20 mL) and the layers separated. The aqueous layer was extracted with EtOAc (2×30 mL) and the combined organic extracts washed with brine (30 mL), dried (MgSO4) and concentrated in vacuo. The residue was dissolved in dioxane (6 mL) and 1,2,3,4-tetrahydro-thieno[3,2-e][1,4]diazepin-5-one (300 mg, 1.78 mmol, 1.0 Eq) was added and the reaction heated at reflux overnight. The reaction was cooled to ambient temperature and the solvent removed in vacuo. The residue was purified by column chromatography (ISCO™ Companion©, 40 g column, 0 to 10% MeOH/DCM) to give the title compound as an off-white solid (178 mg, 0.06 mmol, 33%); 1H NMR (DMSO D6) 1.50 (3H, d), 2.92-2.99 (1H, m), 3.13 (1H, m), 3.20-3.25 (2H, m), 5.32 (1H, dd), 6.91 (1H, d), 7.25-7.35 (2H, m), 7.36-7.41 (2H, m), 7.58 (1H, d), 7.61-7.63 (1H, m); LC/MS M+1 (obs.) 307.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838517B2
Source datasetuspto-grants-2010_11
ORD IDord-a76abb55417644d9a39fec5cd5bcdefe
Source noteuspto-grants-2010_11