HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373189Generated: November 1, 2026
2-Fluorobenzylamine → HCID 21074212, compound
https://huagongshe.com/reaction/1373189
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluorobenzylamine | HCID 66649 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 86594826 | HCID 86594826 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21074212 | HCID 21074212 | 76% |
Reaction Steps
2-(3-isopropyloxy-5-carboxy-benzoyl) amino-5-pyridine carboxylic acid (0.10 g, 0.30 mM), 4A molecular sieves (0.3 g) and 2-fluorobenzylamine were stirred in MeOH at ambient temperature for 2 hrs then sodium cyanoborohydride (0.023 g, 0.36 mM) added. After a further 2 hrs the reaction mixture was filtered, residue washed with MeOH and the filtrate concentrated in vacuo. Water was added, then acidified with 2M HCl to precipitate a colourless solid which was filtered, washed with water and dried under high-vacuum to give the title compound as a light brown solid (00.10 g, 76%); 1H NMR δ (d6-DMSO): 1H NMR δ (d6-DMSO): 1.29 (d, 6H), 4.13 (d, 2H), 4.74 (m, 1H), 7.20–7.30 (m, 3H), 7.43 (m, 1H), 7.58 (m, 2H), 7.68 (s, 1H), 8.28 (s, 2H), 8.87 (s, 1H), 11.10 (bs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07160906B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-dcd142fd6e144922a567d3ef9538575a |
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| Source note | uspto-grants-2007_01 |
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