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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794784Generated: November 3, 2026

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

https://huagongshe.com/reaction/1794784

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, 2 H), 2.59–2.71 (m, 2 H), 4.47–4.50 (m, 1 H), 5.20 (brs, 1 H), 7.31–7.34 (m, 1 H), 7.68–7.71 (m, 1 H), 8.42–8.43 (m, 1 H), 8.50–8.51 (m, 1 H); MS (ES) m/z: 139 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022716B2
Source datasetuspto-grants-2006_04
ORD IDord-cf33eec1fd874d97a738ecb769d72049
Source noteuspto-grants-2006_04