Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | (1-chloro-6-methoxy-isoquinolin-3-yl)-(5-methyl-1H-pyrazol-3-yl)-amine | HCID 57799674 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 136055516 | HCID 136055516 | — |
Reaction Steps
The mixture of (1-chloro-6-methoxy-isoquinolin-3-yl)-(5-methyl-1H-pyrazol-3-yl)-amine (1 g), 40% aq. HBr (15 ml), acetic acid (50 ml) was heated at 120° C. for 8 hours. After reaction finished, the mixture was evaporated to oil and diluted with 20 ml of ethyl acetate. The organic layer was washed with aq. NaHCO3 and was evaporated to give 450 mg of crude 1-Bromo-3-(5-methyl-1H-pyrazol-3-ylamino)-isoquinolin-6-ol by reduced pressure. LC-MS m/e 319(MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572809B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-6e81e0574f904058b8598f20a1157fbc |
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| Source note | uspto-grants-2009_08 |
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