HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080345Generated: October 31, 2026
HCID 11504490, compound → HCID 57736689, compound
https://huagongshe.com/reaction/2080345
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11504490 | HCID 11504490 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57736689 | HCID 57736689 | 82.4% |
Reaction Steps
A solution of N-[(6-fluoro-3′-{[(3S)-3-methyl-1-piperazinyl]methyl}-3-biphenylyl)methyl]-3-(4-piperidinylmethyl)benzamide (100 mg, 0.194 mmol) in THF (2.0 mL) was added to lithium aluminum hydride (1.0 N in THF, 2 mL, 2 mmol). The mixture was heated in a microwave reactor at 80° C. for 60 minutes. After cooling to room temperature, the reaction mixture was carefully quenched with saturated Na2SO4, filtered through celite, dried over K2CO3 and concentrated under vacuum to give a crude oil. Further purification by Gilson reverse phase HPLC, eluting with acetonitrile/water/0.1% TFA (10/90 to 70/30, v/v, over 12 min), gave the title compound (80 mg, 82%) as an oil. LC/MS: m/z, 502 (M+H), 1.29 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07932247B2 |
|---|
| Source dataset | uspto-grants-2011_04 |
|---|
| ORD ID | ord-38cc27f74241456f8f9831e775ef98a6 |
|---|
| Source note | uspto-grants-2011_04 |
|---|