Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Bromomethyl methyl ether | HCID 83093 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67482536 | HCID 67482536 | — |
Reaction Steps
Bromomethyl methyl ether (0.25 mL, 3.06 mmol) was added dropwise to a cold (0° C.) solution of the compound prepared in Part A (0.222 g, 1.79 mmol) and N,N-diisopropylethylamine (0.47 mL, 2.68 mmol) in CH2Cl2 (10 mL). The resulting mixture stirred at 0° C. for 2½ hr, water was added and layers separated. The CH2Cl2 layer was dried over MgSO4, filtered and evaporated in vacuo to give the desired MOM protected amino pyridine product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796313B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-2a446b4c16cd4f90be55056e53b25c40 |
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| Source note | uspto-grants-2014_08 |
|---|