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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789659Generated: October 31, 2026

4-[(2-Methylthio-ethyl)-(2-methoxy-benzoyl)-amino]-benzenesulfonamide → 4-[(2-Methylthio-ethyl)-(2-methoxy-benzyl)-amino]-benzenesulfonamide

https://huagongshe.com/reaction/1789659

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(2-Methylthio-ethyl)-(2-methoxy-benzoyl)-amino]-benzenesulfonamideHCID 22036216—
ReactantHCID 178419153HCID 178419153—
SolventTetrahydrofuranHCID 8028—
Product4-[(2-Methylthio-ethyl)-(2-methoxy-benzyl)-amino]-benzenesulfonamideHCID 2203616777.4%

Reaction Steps

A solution of 1 M BH3.THF/THF (6.8 mL, 6.8 mmol) was added to a solution of 4-[(2-methylthio-ethyl)-(2-methoxy-benzoyl)-amino]-benzenesulfonamide (0.51 g, 1.34 mmol) in THF (5 mL). After 18 h, the excess BH3 was quenched by addition of 0.1 M HCl; followed by partitioning the mixture between CH2Cl2 and NaHCO3. The organic layer was dried (Na2SO4), filtered, evaporated in vacuo, and the residue was purified by MPLC (CH2Cl2 to 70:30 CH2Cl2/EtOAc) to afford 0.38 g (77%) of 4-[(2-methylthio-ethyl)-(2-methoxy-benzyl)-amino]-benzenesulfonamide as a clear glass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071177B2
Source datasetuspto-grants-2006_07
ORD IDord-e17c250301514e26be8bfcb2abe5b00e
Source noteuspto-grants-2006_07