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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273996Generated: October 31, 2026

3-Methoxybenzylamine → HCID 90354256, compound

https://huagongshe.com/reaction/2273996

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxybenzylamineHCID 21156—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromo-3-methylbenzoic acidHCID 82131—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDichloromethaneHCID 6344—
ProductHCID 90354256HCID 90354256—

Reaction Steps

To a solution of 4-bromo-3-methylbenzoic acid (100 mg, 0.465 mmol) in DCM (2 mL) were added (3-methoxyphenyl)methanamine (70.2 mg, 0.512 mmol), DIEA (0.244 mL, 1.395 mmol) and HATU (212 mg, 0.558 mmol) at RT. The reaction was stirred under argon at RT for 1 h. The crude product was purified by normal phase chromatography. 58A was obtained as white solid (155 mg, 0.464 mmol, 100% yield). LCMS (ESI) m/z: 336.0 (M+H)+; 1H NMR (400 MHz, CHLOROFORM-d) δ 7.67 (d, J=2.2 Hz, 1H), 7.57 (d, J=8.4 Hz, 1H), 7.46-7.39 (m, 1H), 7.30-7.24 (m, 1H), 6.92 (dd, J=7.6, 0.6 Hz, 1H), 6.88 (t, J=1.8 Hz, 1H), 6.84 (dt, J=8.1, 1.3 Hz, 1H), 6.38 (br. s., 1H), 4.60 (d, J=5.7 Hz, 2H), 3.80 (s, 3H), 2.43 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126944B2
Source datasetuspto-grants-2015_09
ORD IDord-5d2eac726a094d5c8fd3f6f5f9684160
Source noteuspto-grants-2015_09