HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7794Generated: October 29, 2026
Formaldehyde → 6-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]-N,N-dimethylpyridin-3-amine
https://huagongshe.com/reaction/7794
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 6-[4-(1,3-Benzoxazol-2-yl)-2-methoxyphenyl]pyridin-3-amine | HCID 10149716 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]-N,N-dimethylpyridin-3-amine | HCID 10236912 | — |
Reaction Steps
6-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]pyridin-3-amine (22 mg, 0.070 mmol) was dissolved in MeOH (2 mL), and AcOH (2 drops). NaCNBH3 (44 mg, 0.70 mmol) and formaldehyde (50 μL, 0.70 mmol) were added and the mixture was stirred overnight. The mixture was partitioned between CH2Cl2 and dilute brine. The aqueous layer was extracted with CH2Cl2 (3×15 mL). The combined organic layers were dried over MgSO4, filtered and concentrated. The crude mixture was adsorbed onto silica gel and purified by automated flash chromatography using an EtOAc/hexanes gradient to afford the desired 6-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]-N,N-dimethylpyridin-3-amine: 1H NMR (CDCl3, 300 MHz) δ 8.24–8.23 (d, 1H), 7.94 (s, 2H), 7.87 (s, 1H), 7.84–7.79 (m, 2H), 7.59 (m, 1H), 7.38–7.35 (m, 2H), 7.07–7.06 (m, 1H), 4.01 (s, 3H), 3.04 (s, 6H). MS (ESI) 346 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087601B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-5a63f83402bd4a00a7cdbe18b772ccfe |
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| Source note | uspto-grants-2006_08 |
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