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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470360Generated: October 26, 2026

2-Amino-N-methylbenzamide → N-Methyl-2-(2-phenyl-furo[3,2-b]pyridin-7-ylamino)-benzamide

https://huagongshe.com/reaction/1470360

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-N-methylbenzamideHCID 308072—
Reactant7-Chloro-2-phenyl-furo[3,2-b]pyridineHCID 66779241—
ProductN-Methyl-2-(2-phenyl-furo[3,2-b]pyridin-7-ylamino)-benzamideHCID 66779555—

Reaction Steps

The title compound was prepared by procedure D using 7-chloro-2-phenylfuro[3,2-b]pyridine (50.00 mg; 0.22 mmol; 1.00 eq.) instead of 7-chloro-2-(3,4,5-trimethoxyphenyl)furo[3,2-b]pyridine, and using 2-amino-N-methylbenzamide(39.23 mg; 0.26 mmol; 1.20 eq.) instead of N-(3-aminomethyl-pyridin-2-yl)-N-methyl-methanesulfonamide and was obtained as a white solid (50 mg, 67%). (HPLC (method F): 92%, RT: 3.37 min); MS (m/z) 344 [M+H]+, RT: 2.5 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006440B2
Source datasetuspto-grants-2015_04
ORD IDord-9ff35a444f6744d3b7f50c044c832b18
Source noteuspto-grants-2015_04