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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108988Generated: October 30, 2026

6-chloro-N-(3-methylsulphonylaminobenzyl)nicotinamide → HCID 21914592, compound

https://huagongshe.com/reaction/2108988

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-chloro-N-(3-methylsulphonylaminobenzyl)nicotinamideHCID 21914545—
ReactantN-[4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-3-thiophenecarboxamideHCID 21914662—
ProductHCID 21914592HCID 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, in), 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514456B2
Source datasetuspto-grants-2009_04
ORD IDord-870dd1b9503c46bb8aea44c495c2b8eb
Source noteuspto-grants-2009_04