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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170059Generated: November 1, 2026

5-Bromo-2-methanesulfonylpyridine → HCID 71487974, compound

https://huagongshe.com/reaction/2170059

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-methanesulfonylpyridineHCID 13433424—
ReactantHCID 68653876HCID 68653876—
ReactantHCID 71201914HCID 71201914—
ReactantHCID 84668872HCID 84668872—
ProductHCID 71487974HCID 71487974—

Reaction Steps

Prepared analogously to Compound 1 using IM46 and (S)-1-(6-Methanesulfonyl-pyridin-3-yl)-ethylamine (prepared from 1-(6-Methanesulfonyl-pyridine-3-yl)-ethanone analogously to IM24, which was prepared from commercially available 5-Bromo-2-methanesulfonyl-pyridine CAS 98626-95-0). Yield from IM48=1.54 g (68%). 1H-NMR (500 MHz, DMSO) δ 8.80 (d, 1H), 8.72 (s, 1H), 8.02 (m, 2H), 7.27 (m, 2H), 7.20 (s, 1H), 7.12 (d, 2H), 5.08 (m, 1H), 3.27 (s, 3H), 2.20 (m, 1H), 1.95 (m, 1H), 1.42 (d, 3H), 1.37 (m, 1H), 1.22 (m, 1H), LC-MS (m/z) 345.1 (MH+), tR=1.21 min (method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09050327B2
Source datasetuspto-grants-2015_06
ORD IDord-8c620656d77a415e9d2d9f8c6fe797b7
Source noteuspto-grants-2015_06