HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173030Generated: November 1, 2026
4-Methoxybenzylamine → HCID 68765988, compound
https://huagongshe.com/reaction/1173030
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 11739868 | HCID 11739868 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68765988 | HCID 68765988 | 62.7% |
Reaction Steps
To a mixture of racemic-(trans)-2-{4-[(3-phenoxybenzyl)amino]phenyl}cyclopropanecarboxylic acid (I-2a) (0.14 g, 0.40 mmol) in dichloromethane (3 mL) and DMF (1 mL) was added HATU (0.23 g, 0.60 mmol). The mixture was stirred for 15 min followed by addition of 4-methoxybenzylamine (0.96 g, 0.80 mmol). The solution stirred for 6 h after which the dichloromethane was removed via rotavap. Sat. NaHCO3 and ethyl acetate were added and the organic layer separated and washed with H2O, dried over MgSO4, filtered and concentrated. The resulting oil was triterated with Et2O and formed a white ppt which was filtered and dried under high vacuum to give the title compound as a white powder (0.12 g, 62%). 1H NMR (400 MHz, CDCl3) δ 7.34-7.25 (m, 6H), 7.19-7.07 (m, 5H), 6.99 (t, J=7.9 Hz, 2H), 6.91 (t, J=8.3 Hz, 2H), 6.54 (d, J=8.4 Hz, 2H), 5.78 (s, 1H), 4.42-4.40 (m, 2H); 4.28 (s, 2H), 4.00 (s, 1H), 2.46-2.42 (m, 1H), 2.34 (s, 3H), 1.60-1.55 (m, 1H), 1.48-1.44 (m, 1H), 1.21-1.14 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834013B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-8f8ee82399954849ac467c36a6e68f35 |
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| Source note | uspto-grants-2010_11 |
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