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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105553Generated: October 30, 2026

Methanesulfonyl chloride → HCID 86600479, compound

https://huagongshe.com/reaction/2105553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 69006818HCID 69006818—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86600479HCID 8660047990%

Reaction Steps

To a solution of 3-hydroxymethyl-1-(4-methoxy-benzyl)-1,3,4,5-tetrahydro-benzo[b]azepin-2-one (0.26 mmol) in 2 mL of anhydrous THF at 0° C. is added MsCl (0.39 mmol) and DIEA (0.47 mmol). After the addition, the mixture is allowed to warm up to room temperature and then stirred for 1 hour. The solvent is removed under vacuum and the residue is treated with water (5 mL) and extracted with EtOAc (3×5 mL). The combined organic layers are concentrated and the residue is purified by flash column chromatography (silica gel) to provide methanesulfonic acid 1-(4-methoxy-benzyl)-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-3-ylmethyl ester as white crystals. Yield: 90%. MS: (ES+): 390[M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579363B2
Source datasetuspto-grants-2009_08
ORD IDord-9d0a38069f8746a29748e1db95d0f5e4
Source noteuspto-grants-2009_08