HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 56970630, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 4-methyl-5-(2-piperazin-1-ylethyl)-2-benzofuran-1(3H)-one hydrochloride | HCID 67517229 | — |
| Reactant | 2-(1-Oxo-1,3-dihydroisobenzofuran-5-yl)acetaldehyde | HCID 77231261 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 56970630 | HCID 56970630 | — |
Reaction Steps
A mixture of 4-methyl-5-(2-piperazin-1-ylethyl)-2-benzofuran-1(3H)-one hydrochloride (62 mg, 0.21 mmol), (1-oxo-1,3-dihydro-2-benzofuran-5-yl)acetaldehyde (40 mg, 0.21 mmol), and sodium triacetoxyborohydride (67 mg, 0.32 mmol) in DCM (5 mL) was stirred overnight with a drop of acetic acid. LC showed formation of the desired product, which was purified by mass-directed HPLC (0.1% TFA in water and acetonitrile). LC-MS (IE, m/z): 435 [M+1]+. (0.076 μM)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073882B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-7697c1be201c41a1bda9a39a5f6d95d4 |
| Source note | uspto-grants-2015_07 |