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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173030Generated: November 1, 2026

4-Methoxybenzylamine → HCID 68765988, compound

https://huagongshe.com/reaction/1173030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzylamineHCID 75452—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 11739868HCID 11739868—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 68765988HCID 6876598862.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834013B2
Source datasetuspto-grants-2010_11
ORD IDord-8f8ee82399954849ac467c36a6e68f35
Source noteuspto-grants-2010_11