HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519644Generated: November 3, 2026
Sodium triacetoxyborohydride → HCID 56970864, compound
https://huagongshe.com/reaction/1519644
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 5-[2-(piperazin-1-yl)ethyl]-2-benzofuran-1(3H)-one | HCID 59568671 | — |
| Reactant | HCID 86694487 | HCID 86694487 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 56970864 | HCID 56970864 | — |
Reaction Steps
A solution of crude 2-(cyclopropyloxy)-4-(2-oxoethyl)benzonitrile (80 mg, 0.4 mmol), 5-(2-piperazin-1-ylethyl)-2-benzofuran-1(3H)-one (150 mg, 0.6 mmol) and NaBH(OAc)3 (400 mg, 2 mmol) in 10 mL of anhydrous DCM was stirred at ambient temperature overnight. The reaction mixture was added 50 mL of DCM and washed with brine. The organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified with prep-TLC to afford 2-(cyclopropyloxy)-4-(2-{4-[2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazin-1-yl}ethyl)benzonitrile. 1H-NMR (400 MHz, CDCl3) δ ppm 7.77 (d, J=7.8 Hz, 1H), 7.37 (d, J=7.8 Hz, 1H), 7.31 (d, J=7.8 Hz, 1H), 7.27 (s, 1H), 7.11 (s, 1H), 6.78˜6.80 (m, 1H), 5.22 (s, 2H), 2.42˜2.93 (m, 17H), 0.77˜0.80 (m, 4H). (0.28 μM)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073882B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-dbefc149f9a84692bdfde709030083ee |
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| Source note | uspto-grants-2015_07 |
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