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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061278Generated: November 3, 2026

3-[(2S)-oxiran-2-yl]pyridine → (S)-2-amino-1-(pyridin-3-yl)ethanol

https://huagongshe.com/reaction/1061278

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[(2S)-oxiran-2-yl]pyridineHCID 13319560—
ReactantAmmonium methanolHCID 22220579—
Product(S)-2-amino-1-(pyridin-3-yl)ethanolHCID 40480581—

Reaction Steps

The title compound was prepared from 3-[(2S)-oxiranyl]pyridine (which was obtained in Example 129) and saturated ammonium methanol in substantially the same manner, as described in Example 124. The product was obtained as a brown oil; 1H NMR (400 MHz, DMSO-d6) δ 1.60 (brs, 2H), 2.59-2.71 (m, 2H), 4.47-4.50 (m, 1H), 5.20 (brs, 1H), 7.31-7.34 (m, 1H), 7.68-7.71 (m, 1H), 8.42-8.43 (m, 1H), 8.50-8.51 (m, 1H); MS (ES) m/z: 139 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-271810768904466faf4c2a1484f8ff1b
Source noteuspto-grants-2003_02