2-(3-Aminophenyl)ethanesulfonamide → 2-[3-((4-(2-Methoxyphenyl)pyridin-2-yl)amino)phenyl]-ethanesulfonamide

Participants

Role	Name	HCID	Charge
Reactant	2-(3-Aminophenyl)ethanesulfonamide	HCID 58236871	—
Reactant	2-Chloro-4-(2-methoxyphenyl)pyridine	HCID 58432611	—
Product	2-[3-((4-(2-Methoxyphenyl)pyridin-2-yl)amino)phenyl]-ethanesulfonamide	HCID 60197052	2.3%

Reaction Steps

H1 was prepared from A6 (92 mg, 0.46 mmol) and A1 (100 mg, 0.46 mmol) following the procedure reported for G1 and obtained as a pale yellow amorphous solid (4 mg, 2%). 1H NMR (400 MHz, d6-DMSO, 300K) δ 2.95-3.03 (m, 2H), 3.21-3.29 (m, 2H), 3.81 (s, 3H), 6.87 (bs, 2H), 6.93-7.01 (m, 2H), 7.07 (t, J=7.5 Hz, 1H), 7.10-7.14 (m, 1H), 7.16 (d, J=8.5 Hz, 1H), 7.29 (t, J=8.0 Hz, 1H), 7.36-7.47 (m, 4H), 8.07 (d, J=5.4 Hz, 1H), 9.67 (bs, 1H). MS (ES) C20H21N3O3S requires: 383. found: 384 (M+H)+.

Provenance & Evidence

DOI	10.6084/m9.figshare.5104873.v1
Patent number	US09242937B2
Source dataset	uspto-grants-2016_01
ORD ID	ord-be3240dc06cf4161ac7154f6e9d74071
Source note	uspto-grants-2016_01