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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824276Generated: November 2, 2026

Triethylamine → HCID 58583287, compound

https://huagongshe.com/reaction/1824276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,6-DichloropyrazineHCID 78504—
Reactant(1R,2S)-(+)-cis-1-Amino-2-indanolHCID 2725045—
Solvent1-ButanolHCID 263—
ProductHCID 58583287HCID 5858328757%

Reaction Conditions

Temperature115 °C

Reaction Steps

To a solution of 2,6-dichloropyrazine (5.0 g, 34 mmol) in n-BuOH (30 mL) was added triethylamine (6.8 g, 9.4 mL, 67 mmol) and (1R,2S)-(+)-cis-1-amino-2-indanol (5.0 g, 34 mmol). The mixture was heated at 115° C. overnight. The solution was cooled to rt and concentrated. Dissolve material in EtOAc (200 mL) and remove insoluble material by vacuum filtration. Wash filtrate sequentially with 4 N NaOH and sat. aq. NaCl. Dry organic extract over MgSO4, filter and concentrate. Purify by biotage MPLC (90 g column, 10% ethyl acetate/hexanes) to afford 4.85 g (57%) of (1R,2S)-1-[(6-chloropyrazin-2-yl)amino]-2,3-dihydro-1H-inden-2-ol as a solid: 1H NMR (CDCl3) δ 2.83–2.87, 3.08–3.13, 3.32, 4.54, 5.11, 5.28–5.31, 7.18–7.28, 7.73, 8.12; MS (ESI+) for C13H12ClN3O m/z 262 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041672B2
Source datasetuspto-grants-2006_05
ORD IDord-06766ed653f74ac6a2f054822e34a5b8
Source noteuspto-grants-2006_05