HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519328Generated: November 4, 2026
4-Fluorobenzylamine → HCID 71538051, compound
https://huagongshe.com/reaction/1519328
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | HCID 86679835 | HCID 86679835 | — |
| Product | HCID 71538051 | HCID 71538051 | 84% |
Reaction Steps
Using the conditions of General Procedure E for Amide Coupling in Parallel Mode, 4-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-biphenyl-2,4′-dicarboxylic acid 2-methyl ester (which may be prepared as described for Intermediate 8; 100 mg, 0.21 mmol) was reacted with 4-fluorobenzylamine (available from Aldrich Chemical Company, Inc.; 78 mg, 0.62 mmol). The resulting ester was hydrolyzed and the acid was purified using HPLC Purification Conditions B to give 4-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-4′-(4-fluoro-benzylcarbamoyl)-biphenyl-2-carboxylic acid (88 mg, 84%). 1H NMR (400 MHz, DMSO-d6) δ ppm 13.17 (br s, 1H), 9.11 (t, J=5.8 Hz, 1H), 8.46 (s, 1H), 8.38 (s, 1H), 8.33 (s, 1H), 8.24 (d, J=7.8 Hz, 1H), 8.09 (d, J=8.3 Hz, 1H), 7.96 (d, J=8.0 Hz, 2H), 7.76 (d, J=8.5 Hz, 1H), 7.59 (d, J=8.0 Hz, 1H), 7.50 (d, J=8.0 Hz, 2H), 7.35-7.41 (m, 2H), 7.16 (t, J=8.7 Hz, 2H), 4.50 (d, J=5.8 Hz, 8H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073881B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-13d095121d704d059a54399c0450d463 |
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| Source note | uspto-grants-2015_07 |
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