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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220189Generated: October 28, 2026

4-Bromoaniline → HCID 59238276, compound

https://huagongshe.com/reaction/220189

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanilineHCID 7807—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHydrochloride methanolHCID 21893726—
ReactantHCID 59238302HCID 59238302—
SolventDichloromethaneHCID 6344—
ProductHCID 59238276HCID 59238276—

Reaction Steps

To a solution of (E)-2-{4-[2-(2-tert-butoxycarbonylamino-phenylcarbamoyl)-vinyl]-phenyl}-4-(1-methyl-pyrrolidin-2-yl)-butyric acid (2.54 g, 5 mmol), Et3N (1.21 g, 10 mmol), and HATU (3.80 g, 10 mmol) in CH2Cl2 (30 mL) was added 4-bromo-phenylamine (1.29 g, 7.5 mmol). This mixture was stirred overnight at room temperature and then evaporated. The mixture redissolved in 20 mL of EtOAc and washed with 2N HCl (20 mL×3), brine, 5% NaHCO3 (20 mL×3), brine, dried with Na2SO4, filtered and evaporated. The residue was purified by column chromatography on silica gel using hexane/EtOAc to give a white solid. 1.25 M HCl/MeOH (4 mL) was added to the product. The solution was stirred for 4 h at ambient temperature. After reaction, the solution was neutralized with solid NaHCO3. The final product was obtained by preparative HPLC. MS: calc'd 561 (MH+), exp 561 (MH+). 1H NMR (d6-DMSO, 400 MHz), 10.25 (d, 1H, J=8.8 Hz), 9.40 (s, 1H), 7.60-7.56 (m, 4H), 7.53 (d, 1H, J=15.6 Hz), 7.49-7.45 (m, 4H), 7.34 (d, 1H, J=8.0 Hz), 6.93 (d, 1H, J=7.6 Hz), 6.88 (d, 1H, J=15.6 Hz), 6.75 (d, 1H, J=7.6 Hz), 6.58 (t, 1H, J=8.0 Hz), 4.95 (s, 2H), 3.71 (broad s, 1H), 3.07 (broad s, 1H), 2.31 (broad s, 4H), 1.99 (broad s, 2H), 1.69-1.46 (broad m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202866B2
Source datasetuspto-grants-2012_06
ORD IDord-e38872ae4d66410e8b3040d99efacaa8
Source noteuspto-grants-2012_06