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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076645Generated: October 26, 2026

N-(3-iodophenyl)methanesulfonamide → tert-Butyl 2-hydroxy-6-[({3'-[(methylsulfonyl)amino]-1,1'-biphenyl-4-yl}oxy)methyl]-3-(trifluromethyl)benzoate

https://huagongshe.com/reaction/2076645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-iodophenyl)methanesulfonamideHCID 21830928—
ReactantTert-butyl 2-hydroxy-6-{[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]methyl}-3-(trifluoromethyl)benzoateHCID 67119153—
Producttert-Butyl 2-hydroxy-6-[({3'-[(methylsulfonyl)amino]-1,1'-biphenyl-4-yl}oxy)methyl]-3-(trifluromethyl)benzoateHCID 86617412—

Reaction Steps

According to a method similar to Example (31), from N-(3-iodophenyl)methanesulfonamide (134 mg, 0.45 mmol) obtained in Example (35-1) and tert-butyl 2-hydroxy-6-{[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]methyl}-3-(trifluoromethyl)benzoate (250 mg, 0.51 mmol) obtained in Example (22-4), the title compound was obtained as a pale violet powder (20 mg, yield: 8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923573B2
Source datasetuspto-grants-2011_04
ORD IDord-5b2c1707556247889dfe0565ce1247f1
Source noteuspto-grants-2011_04