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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266583Generated: October 31, 2026

Benzyl Bromide → HCID 91357348, compound

https://huagongshe.com/reaction/1266583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 91535710HCID 91535710—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 91357348HCID 91357348—

Reaction Steps

(2R)-3-methyl-2-[(2-ethylthiobenzthiazol-6-sulfonyl)amino]butanoic acid methylester (0.16 g, 0.376 mmol) prepared in a similar manner as in Example 14 was dissolved in DMF (1 mL). K2CO3 (150 mg, 3 equi.) and benzylbromide (0.056 mL, 1.3 equi.) were added at RT. After stirring the reaction solution for 1 hour at RT, ethylacetate (5 mL) and H2O were added to afford the phase separation, when starting material was exhausted. The separated organic phase was washed with H2O for several times, dried over MgSO4 and distilled under reduced pressure to prepare the titled compound, (2R)-3-methyl-2-[(ethylthio-6-benzthiazolsulfonyl)benzylamino]butanoic acid methylester (180 mg, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548667B2
Source datasetuspto-grants-2003_04
ORD IDord-7301828c72f54dd1953d161dce23581c
Source noteuspto-grants-2003_04