HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407862Generated: October 30, 2026
Cyclohexanemethylamine → HCID 59352443, compound
https://huagongshe.com/reaction/1407862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexanemethylamine | HCID 76688 | — |
| Reactant | 2-Fluoro-5-methylaniline | HCID 262970 | — |
| Reactant | 3-[(2'-oxo-5,6-dihydrospiro[benzo[1,2-b:5,4-b']difuran-3,3'-indol]-1'(2'H)-yl)methyl]benzoic acid | HCID 59352253 | — |
| Reactant | 2-[(2'-oxo-5,6-dihydrospiro[benzo[1,2-b:5,4-b']difuran-3,3'-indol]-1'(2'H)-yl)methyl]benzoic acid | HCID 59352308 | — |
| Product | HCID 59352443 | HCID 59352443 | — |
Reaction Steps
Following the procedure as described in EXAMPLE 12 and making non-critical variations using 2-fluoro-5-methylaniline to replace cyclohexanemethylamine, and 2-[(2′-oxo-5,6-dihydrospiro[benzo[1,2-b:5,4-b′]difuran-3,3′-indol]-1′(2′H)-yl)methyl]benzoic acid to replace 3-[(2′-oxo-5,6-dihydrospiro[benzo[1,2-b:5,4-b′]difuran-3,3′-indol]-1′(2′H)-yl)methyl]benzoic acid, N-(2-fluoro-5-methylphenyl)-2-[(2′-oxo-5,6-dihydrospiro[benzo[1,2-b:5,4-b′]difuran-3,3′-indol]-1′(2′H)-yl)methyl]benzamide was obtained (77%) as a colorless solid: mp 214-216° C.; 1H NMR (300 MHz, CDCl3) δ8.25-8.06 (m, 2H), 7.65-7.57 (m, 1H), 7.47-7.33 (m, 2H), 7.33-7.26 (m, 1H), 7.22-7.12 (m, 2H), 7.07-6.86 (m, 4H), 6.46 (s, 1H), 6.40 (s, 1H), 5.27 (s, 2H), 4.95 (d, J=9.0 Hz, 1H), 4.68 (d, J=9.0 Hz, 1H), 4.52 (t, J=8.7 Hz, 2H), 2.96 (t, J=8.5 Hz, 2H), 2.36 (s, 3H); MS (ES+) m/z 543.1 (M+23).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916580B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-57e7007a9b654b79876bc3fd083732bc |
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| Source note | uspto-grants-2014_12 |
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