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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824284Generated: October 26, 2026

methyl 3-bromo-6-{[(1R,2S)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]amino}pyrazine-2-carboxylate → (1R,2S)-1-[(5-bromo-6-methoxypyrazin-2-yl)amino]-2,3-dihydro-1H-inden-2-ol

https://huagongshe.com/reaction/1824284

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 3-bromo-6-{[(1R,2S)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]amino}pyrazine-2-carboxylateHCID 58583440—
Reactantmethyl(1R,2S)-1-[(6-methoxypyrazin-2-yl)amino]-2,3-dihydro-1H-inden-2-olHCID 69664630—
Product(1R,2S)-1-[(5-bromo-6-methoxypyrazin-2-yl)amino]-2,3-dihydro-1H-inden-2-olHCID 58631232—

Reaction Steps

Following the procedure for the preparation of methyl 3-bromo-6-{[(1R,2S)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]amino}pyrazine-2-carboxylate but substituting methyl(1R,2S)-1-[(6-methoxypyrazin-2-yl)amino]-2,3-dihydro-1H-inden-2-ol and making non-critical variations provided the title compound as a solid: 1H NMR (CDCl3) δ 2.07, 3.03–3.07, 3.25–3.30, 3.98, 4.76, 5.38, 7.26–7.32, 7.45; MS (ESI+) for C14H14BrN3O2 m/z 336 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041672B2
Source datasetuspto-grants-2006_05
ORD IDord-11d6c2d7fed24dcbbc95231c57b75367
Source noteuspto-grants-2006_05