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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786650Generated: October 30, 2026

Benzoyl chloride → HCID 66769624, compound

https://huagongshe.com/reaction/1786650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantHCID 66769815HCID 66769815—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66769624HCID 6676962452%

Reaction Steps

{3-[(3-Aminomethyl-benzofuran-5-sulfonyl)-isobutyl-amino]-1-benzyl-2-hydroxy-propyl}-carbamic acid hexahydro-furo[2,3-b]furan-3-yl ester from the previous step (20 mg, 33 umol) was dissolved in 0.5 mL THF. 5.8 uL (50 umol) benzoyl chloride and 7 uL (50 umol) triethylamine were added and the reaction was stirred at room temperature for 1 h. The reaction mixture was purified by prep TLC on the silica gel plate with ethyl acetate/hexanes=2/1 to afford 12 mg (17 umol, 52%) of product. MS 706 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507763B2
Source datasetuspto-grants-2009_03
ORD IDord-0b020d2e3819488f85be6834a110dbfb
Source noteuspto-grants-2009_03