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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642608Generated: October 30, 2026

Acetyl chloride → HCID 66756938, compound

https://huagongshe.com/reaction/1642608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 66757115HCID 66757115—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 66756938HCID 66756938—

Reaction Steps

To a solution of 5-[4-(2-aminobenzyl)-2-benzyloxyphenyl]-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-one (Example 4, Step A) (250 mg, 0.478 mmol) in pyridine (1.5 mL) is added acetylchloride (41 mg, 0.525 mmol). The mixture is stirred at ambient temperature for 30 min., then diluted with EtOAc and washed with 0.5N HCl, saturated NaHCO3 and brine. It is then dried over Na2SO4/MgSO4, filtered and concentrated to afford N-(2-{3-benzyloxy-4-[1,1,4-trioxo-5-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-2-yl]-benzyl}-phenyl)-acetamide as a gum: MS (M+H)+=566.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119666B2
Source datasetuspto-grants-2012_02
ORD IDord-cdd4d243af7f424c9336dacab5c01f56
Source noteuspto-grants-2012_02