Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | 2-(Aminomethyl)-4-methyl-3-pyridinemethanol | HCID 44191037 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | HCID 67077477 | HCID 67077477 | — |
Reaction Steps
A solution of isobutyryl chloride (29 μL, 0.276 mmol) in DCM (0.20 mL) was added to a vigorously stirred mixture of (2-aminomethyl-4-methyl-pyridin-3-yl)-methanol (30 mg, 0.20 mmol) in DCM (1.0 mL) and aqueous Na2CO3 (1 M, 1 mL) at 0° C. After stirring for 30 min at 0° C., DCM (10 mL) and water (1 mL) was added, and the aqueous layer was extracted with DCM (1×10 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (elution with MeOH/DCM 1:20) to give the title compound. MS (m/z): 223.0 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410134B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-bad5aab4e1644cf39c9e731e298f8ee3 |
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| Source note | uspto-grants-2013_04 |
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