HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717841Generated: October 29, 2026
HCID 58515929, compound → HCID 178473887, compound
https://huagongshe.com/reaction/717841
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 58515929 | HCID 58515929 | — |
| Reactant | HCID 178419477 | HCID 178419477 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178473887 | HCID 178473887 | 44% |
Reaction Steps
A mixture of 1-[5-(4-acetylpiperazin-1-yl)-8-chloroimidazo[1,5-a]pyridin-6-yl]ethanamine (11.2 mg, 0.035 mmol), 6-bromo-9H-purine (14 mg, 0.070 mmol) and IV, N-diisopropylethylamine (18 μL, 0.10 mmol) in ethanol (0.93 mL) was heated to 110° C. overnight. Purification by preparative LCMS (pH 10) gave the desired compound (6.7 mg, 44%). LCMS calculated for C20H23ClN9O (M+H)+: m/z=440.2. found: 439.9. 1H NMR (300 MHz, DMSO-d6): δ 8.52 (s, 1H), 8.17 (m, 3H), 7.42 (s, 1H), 7.37 (s, 1H), 5.90 (s, 1H), 3.80 (m, 2H), 3.65 (m, 2H), 3.50 (m, 1H), 3.40 (m, 2H), 3.20 (m, 2H), 2.09 (s, 3H), 1.52, (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193721B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-903488484d0740e598f24a02288398bf |
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| Source note | uspto-grants-2015_11 |
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