Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503359Generated: October 25, 2026

Water → 6-Bromo-3-iodo-N-isobutylimidazo[1,2-a]pyrazin-8-amine

https://huagongshe.com/reaction/1503359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsobutylamineHCID 6558—
Reactant6-Bromo-3-iodo-8-(methylsulfonyl)imidazo[1,2-a]pyrazineHCID 71534042—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product6-Bromo-3-iodo-N-isobutylimidazo[1,2-a]pyrazin-8-amineHCID 7153404477.52%

Reaction Steps

To a stirred solution of 6-bromo-3-iodo-8-methanesulfonyl-imidazo[1,2-a]pyrazine (5.08 g, 12.64 mmol) in NMP (100 mL) was added 3.77 mL isobutylamine (2.77 g, 37.90 mmol, 3 eq) in one portion at rt. After stirring for 2 h at rt, 500 mL water was added and the mixture was extracted with ethyl acetate (3×200 mL). The organic phase was filtered, evaporated and the residue was recrystallized from MeOH/water to yield 3.87 g (77.52%) (6-bromo-3-iodo-imidazo[1,2-a]pyrazin-8-yl)-isobutyl-amine: 1H-NMR (300 MHz, d6-DMSO): δ=8.09 (1H, tr), 7.60 (1H, s), 7.54 (1H, s), 3.19 (2H, dd), 1.95 (1H, m), 0.85 (6H, d) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212184B2
Source datasetuspto-grants-2015_12
ORD IDord-331ea62163bc426bac8e18b6ada1eb16
Source noteuspto-grants-2015_12