HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Isobutyraldehyde | HCID 6561 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 4-(4-amino-1H-benzimidazol-1-yl)benzonitrile | HCID 68386848 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}benzonitrile | HCID 68386517 | 62.3% |
Reaction Steps
To a stirred solution of 4-(4-amino-1H-benzimidazol-1-yl)benzonitrile (246 mg, 1.05 mmol) in dichloromethane (10 mL) at rt was added sodium triacetoxy borohydride (311 mg, 1.47 mmol, 1.4 eq), isobutyraldehyde (91 mg, 1.26 mmol, 1.2 eq) and acetic acid (63 m g, 1.05 mmol, 1 eq) and the mixture was stirred for 2 h. The mixture was poured on water and extracted with DCM. After evaporation of the organic phase, purification of the residue by flash chromatography yielded 190 mg 4-{4-[(2-methylpropyl)amino]-1H-benzimidazol-1-yl}benzonitrile (62.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09388140B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-14149e3fd1da4d5a8482be05af6d9a95 |
| Source note | uspto-grants-2016_07 |