HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 57537637, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57537502 | HCID 57537502 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57537637 | HCID 57537637 | 57.1% |
Reaction Steps
Sodium borohydride (85.5 mg, 2.25 mmol) was added to methanol (5 mL) at 0° C. After 5 min., 2-(2-amino-5-bromo-pyridin-3-yl)-N,N-dimethyl-2-oxo-acetamide (408 mg, 1.50 mmol) in MeOH (15 mL) was added. After 1 h, the reaction was quenched by addition of saturated NH4Cl and the mixture was concentrated in vacuo. The residue was extracted with ethyl acetate, dried over Na2SO4 and purified by silica gel chromatography using DCM and MeOH to afford 2-(2-amino-5-bromo-pyridin-3-yl)-2-hydroxy-N,N-dimethyl-acetamide (234 mg, 57.1%) as a brown oily solid. The material was used in the next step. MS: m/z 274 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242280B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-6b074749ed1a46eab519f8a9d6ed600f |
| Source note | uspto-grants-2012_08 |