HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-chloro-N-(3-methylsulphonylaminobenzyl)nicotinamide → HCID 21914592, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-chloro-N-(3-methylsulphonylaminobenzyl)nicotinamide | HCID 21914545 | — |
| Reactant | N-[4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-3-thiophenecarboxamide | HCID 21914662 | — |
| Product | HCID 21914592 | HCID 21914592 | — |
Reaction Steps
N-(3-Methylsulphonylaminobenzyl)-6-[5-(thiophen-3-ylcarbonylamino)-2-methyl-phenyl]-nicotinamide was prepared from 6-chloro-N-(3-methylsulphonylaminobenzyl)nicotinamide (Intermediate 4) and N-[4-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]thiophene-3-amide (Intermediate 14) using General Method B. LCMS: retention time 3.03 min, MH+ 521. NMR: δH [2H6]-DMSO 10.12,(1H, s), 9.33,(1H, t), 9.15,(1H, s), 8.78,(1H b), 8.36–8.32,(2H, m), 7.86,(1H, s), 7.78,(1H, d), 7.69–7.65,(3H, m), 7.31,(2H, m), 7.21,(1H, s), 7.11,(2H, m), 4.51,(2H, d), 2.99,(3H, s), 2.32,(3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07125898B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-64f9852061084a9f8cc8ba7d80178a40 |
| Source note | uspto-grants-2006_10 |