HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(3-iodophenyl)methanesulfonamide → tert-Butyl 2-hydroxy-6-[({3'-[(methylsulfonyl)amino]-1,1'-biphenyl-4-yl}oxy)methyl]-3-(trifluromethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(3-iodophenyl)methanesulfonamide | HCID 21830928 | — |
| Reactant | Tert-butyl 2-hydroxy-6-{[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]methyl}-3-(trifluoromethyl)benzoate | HCID 67119153 | — |
| Product | tert-Butyl 2-hydroxy-6-[({3'-[(methylsulfonyl)amino]-1,1'-biphenyl-4-yl}oxy)methyl]-3-(trifluromethyl)benzoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07923573B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-5b2c1707556247889dfe0565ce1247f1 |
| Source note | uspto-grants-2011_04 |