Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86728277 | HCID 86728277 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 71295574 | HCID 71295574 | 85% |
Reaction Steps
2-(5-bromo-2-hydroxyphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde (0.19 g, 0.63 mmol) was dissolved in MeOH (2 mL) at 0° C. NaBH4 (0.072 g, 1.9 mmol) was added portionwise. After addition, the mixture was stirred at 25° C. for 30 minutes, and then H2O (20 mL) was added by dropwise. Extracted with EtOAc (3*50 mL), washed by brine (50 mL). After concentrated, the resulting residue was purified using Prep-TLC (petroleum ether:EtOAc=3:1) to provide 4-bromo-2-(3-(hydroxymethyl)imidazo[1,2-a]pyridin-2-yl)phenol (150 mg, yield: 85%). 1H-NMR (CDCl3, 400 MHz) δ 8.33˜8.35 (m, 1H), 7.72 (s, 1H), 7.62˜7.64 (m, 1H), 7.31˜7.37 (m, 2H), 6.92˜7.01 (m, 2H), 5.20 (s, 2H). MS (M+H)+: 319/321.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09265773B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-63ca7e3c28624b758cd821e460a6d2a1 |
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| Source note | uspto-grants-2016_02 |
|---|