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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31283Generated: October 26, 2026

6-[2-(2,4-Difluorophenyl)chroman-6-yloxy]-pyridin-3-ylamine → N-{6-[2-(2,4-difluorophenyl)chroman-6-yloxy]pyridin-3-yl}methane sulfonamide

https://huagongshe.com/reaction/31283

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-[2-(2,4-Difluorophenyl)chroman-6-yloxy]-pyridin-3-ylamineHCID 17978470—
ReactantN-[6-(2-phenylchroman-6-yloxy)pyridin-3-yl]methanesulfonamideHCID 17978472—
ProductN-{6-[2-(2,4-difluorophenyl)chroman-6-yloxy]pyridin-3-yl}methane sulfonamideHCID 17978551—

Reaction Steps

N-{6-[2-(2,4-difluorophenyl)chroman-6-yloxy]pyridin-3-yl}methane sulfonamide was prepared as described for N-[6-(2-phenylchroman-6-yloxy)pyridin-3-yl]methane sulfonamide in Example 46 starting from 100 mg of 6-[2-(2,4-difluorophenyl)chroman-6-yloxy]-pyridin-3-ylamine (Example 70). The product was crystallised from a mixture of methanol and diethyl ether. 1H NMR (400 MHz, d6-DMSO) δ: 9.67 (s, 1H), 7.99 (d, 1H, J 2.8 Hz), 7.67 (dd, 1H, J 8.8, 2.8 Hz), 7.60 (m, 1H), 7.30 (m, 1H), 7.16 (m, 1H), 6.98 (d, 1H, J 8.8 Hz), 6.92-6.86 (m, 3H), 5.31 (dd, 1H, J 10.3, 2.3 Hz), 3.01 (m, 1H), 2.98 (s, 3H), 2.76 (m, 1H), 2.16 (m, 1H), 2.06 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425568B2
Source datasetuspto-grants-2008_09
ORD IDord-25846f1e22ff474d934070f01cc4ff25
Source noteuspto-grants-2008_09