HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828111Generated: November 1, 2026
o-Fluorobenzaldehyde → HCID 22064650, compound
https://huagongshe.com/reaction/1828111
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 22064712 | HCID 22064712 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22064650 | HCID 22064650 | 76% |
Reaction Steps
(RS)-N-(2-amino-4-cyano-benzyl)-2-ethoxy-2-(4-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetamide (0.060 g) was treated in MeOH (1 ml) successively with 2-fluoro-benzaldehyde (56 mg) and 1 ml of a MeOH-solution containing scrupulously dried ZnCl2 (83 mg) and NaCNBH3 (29 mg). The reaction mixture was stirred for 6 h at 50–55° C., poured onto crashed ice and extracted two times with ethyl acetate. The combined organic layers were washed with water and brine and dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography (silica gel, hexane/AcOEt=6/4) to yield (RS)-N-[4-cyano-2-(2-fluoro-benzylamino)-benzyl ]-2-ethoxy-2-(4-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetamide (58 mg) as yellow oil, MS 505.4 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07056932B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-db8aa210a3b24b2eb7e2548c1e2f2400 |
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| Source note | uspto-grants-2006_06 |
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