HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640554Generated: October 29, 2026
Ammonia → 3-Cyclobutyl-1-iodoimidazo[1,5-a]pyrazin-8-amine
https://huagongshe.com/reaction/1640554
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | 8-Chloro-3-cyclobutyl-1-iodoimidazo[1,5-a]pyrazine | HCID 42609364 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 3-Cyclobutyl-1-iodoimidazo[1,5-a]pyrazin-8-amine | HCID 42609365 | — |
Reaction Steps
A Parr bomb containing 8-chloro-3-cyclobutyl-1-iodoimidazo[1,5-a]pyrazine (759 mg, 2.3 mmol) in IPA (100 mL) was saturated with NH3(g) for 5 min at 0° C. then sealed and heated at 115° C. for 38 h. The reaction mixture was then concentrated under reduced pressure, partitioned between DCM (200 mL) and H2O (50 mL) and extracted with DCM (50 mL). Combined organic fractions were washed with brine, dried (Na2SO4) and concentrated under reduced pressure to provide the title compound as a white solid; 1H NMR (400 MHz, CDCl3) δ 7.13 (d, J=4.8 Hz, 1H), 7.01 (d, J=5.2 Hz, 1H), 5.63 (br, 2H), 3.73 (quintetd, J=0.8 Hz, 8.4 Hz, 1H), 2.60-2.38 (m, 4H), 2.20-1.90 (m, 2H); MS (ES+): m/z 315.9 (100) [MH+]; HPLC: tR=1.75 min (OpenLynx, polar—5 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08114846B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-151625e24ebd4feda6ec691db470ce8b |
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| Source note | uspto-grants-2012_02 |
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