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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201516Generated: October 29, 2026

Aniline → HCID 117771515, compound

https://huagongshe.com/reaction/2201516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 87131485HCID 87131485—
SolventDimethylformamideHCID 6228—
ProductHCID 117771515HCID 11777151593.2%

Reaction Steps

To a solution of 3-(benzyloxy)-6-bromopicolinic acid (0.50 g, 1.62 mmol) and HATU (1.23 g, 3.24 mmol) in DMF (5 mL) was added phenylamine (0.52 g, 4.87 mmol) dropwise. After stirring at room temperature overnight, the mixture was concentrated and the residue was diluted with water and extracted with EtOAc. The combined organic phase was washed with brine, dried over Na2SO4 and concentrated. The residue was purified by flash gel chromatography (DCM:MeOH=50:1) to afford the product of N-benzyl-3-(benzyloxy)-6-bromopicolinamide (0.60 g, yield: 93.2%). 1H-NMR (CDCl3, 400 MHz) δ 7.79 (br s, 1H), 7.38˜7.41 (m, 3H), 7.19˜7.32 (m, 9H), 5.18 (s, 2H), 4.58 (d, J=5.6 Hz, 2H). MS (M+H)+: 397/399.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364482B2
Source datasetuspto-grants-2016_06
ORD IDord-e087835338984d098a7b07d2fdf25c36
Source noteuspto-grants-2016_06