HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014710Generated: October 31, 2026
6-Bromo-1-((tetrahydro-2H-pyran-4-yl)methyl)-1H-imidazo[4,5-b]pyrazin-2(3H)-one → HCID 178432081, compound
https://huagongshe.com/reaction/1014710
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Bromo-1-((tetrahydro-2H-pyran-4-yl)methyl)-1H-imidazo[4,5-b]pyrazin-2(3H)-one | HCID 86626395 | — |
| Reactant | HCID 86761360 | HCID 86761360 | — |
| Reactant | HCID 178432082 | HCID 178432082 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178432081 | HCID 178432081 | 6.5% |
Reaction Steps
6-(2-Methyl-1H-benzo[d]imidazol-5-yl)-1-((tetrahydro-2H-pyran-4-yl)methyl)-1H-imidazo[4,5-b]pyrazin-2(3H)-one hydrochloride. tert-Butyl 2-methyl-6-(trimethylstannyl)-1H-benzo[d]imidazole-1-carboxylate (120 mg, 0.30 mmol), 6-bromo-1-((tetrahydro-2H-pyran-4-yl)methyl)-1H-imidazo[4,5-b]pyrazin-2(3H)-one (See Example 101.B) (96 mg, 0.3 mmol), dichlorobis(triphenylphosphine)palladium(II) (21 mg, 0.03 mmol) in DMF (5 mL) were reacted for 1.5 h at 90° C. The product was purified by reverse-phase semi-preparatory HPLC (10-100% acetonitrile+0.1% TFA in H2O+0.1% TFA, over 30 min). The desired fractions were concentrated, and treated with 4N hydrochloric acid in diethyl ether (few drops), sonicated and concentrated. This procedure was repeated twice more to provide the title compound (8 mg, 6.5% yield). 1H NMR (400 MHz, DMSO-d6) 12.12 (s, 1H), 8.62 (s, 1H), 8.31 (s, 1H), 8.15 (d, J=8.4, 1H), 7.82 (d, J=8.4, 1H), 3.85 (m, 2H), 3.81 (d, J=8.0, 2H), 3.26 (t, J=11.2, 2H), 1.90 (m, 1H), 1.61 (m, 2H), 1.35-1.23 (m, 3H), 0.89-0.86 (m, 2H); MS (ESI) m/z 365.1 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981893B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-7b140bd61dcd4f28a10378751eb0930f |
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| Source note | uspto-grants-2011_07 |
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