HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57551Generated: October 26, 2026
Hydrogen Bromide → 5-bromo-N-methyl-N-(tetrahydro-2H-pyran-4-yl)pyridin-2-amine
https://huagongshe.com/reaction/57551
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | N2-methyl-N2-(tetrahydro-2H-pyran-4-yl)-2,5-Pyridinediamine | HCID 43610738 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-bromo-N-methyl-N-(tetrahydro-2H-pyran-4-yl)pyridin-2-amine | HCID 55137965 | — |
Reaction Steps
To a solution of N2-methyl-N2-(tetrahydro-2H-pyran-4-yl)pyridine-2,5-diamine (150 mg, 0.73 mmol) in 2 mL of aq HBr was added a solution of NaNO2 (55 mg, 0.80 mmol) in 1 mL of H2O at 0° C. Then the mixture was stirred at 0° C. for 40 minutes. After that, the mixture was poured into a solution of CuBr (220 mg, 1.53 mmol) in 2 mL aq HBr at 0° C., the reaction was heated to 60° C. and stirred for 2 hours. After cooling, the mixture was based with 2M NaOH to pH=8-9 and extracted with EA, washed with H2O and brine, dried and concentrated, purified on TLC (EA:PE=1:1) to give white solid. MS (m/z): 273 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434726B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-92f8ad19765a4c6d83f297479fb24959 |
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| Source note | uspto-grants-2016_09 |
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