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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824283Generated: November 2, 2026

Sodium Bicarbonate → HCID 58631219, compound

https://huagongshe.com/reaction/1824283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 58583287HCID 58583287—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 58631219HCID 5863121971%

Reaction Steps

To a solution of (1R,2S)-1-[(6-chloropyrazin-2-yl)amino]-2,3-dihydro-1H-inden-2-ol (2 g, 7.6 mmol) in MeOH (26 mL) was added a solution of NaOMe (1.3 g, 23 mmol) in MeOH (40 mL). The mixture was heated at reflux for 24 hr. Additional NaOMe (1.3 g) was added. Continue heating at reflux for 24 hr, and then add additional NaOMe (1.3 g). Continue heating at reflux for 24 hr and cool to rt. Dilute with EtOAc and was with sat. aq. NaHCO3. The solids were removed by filtration. Separate phases and wash organic extract with additional sat. aq. NaHCO3. Dry organic extracts over MgSO4, filter and concentrate. Purify by biotage MPLC (90 g column, 25% ethyl acetate/hexanes) to afford 1.4 g (71%) of (1R,2S)-1-[(6-methoxypyrazin-2-yl)amino]-2,3-dihydro-1H-inden-2-ol as an oil: 1H NMR (CDCl3) δ 3.04–3.08, 3.23–3.29, 3.91, 4.75–4.78, 5.18, 5.42–5.45, 7.25–7.34, 7.57–7.61; MS (ESI+) for C14H15N3O2 m/z 258 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041672B2
Source datasetuspto-grants-2006_05
ORD IDord-ff2110594123498096202955682f8f0e
Source noteuspto-grants-2006_05