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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874878Generated: November 2, 2026

Diisopropylethylamine → HCID 178440106, compound

https://huagongshe.com/reaction/1874878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 59451460HCID 59451460—
ReactantHCID 178440112HCID 178440112—
SolventDimethylformamideHCID 6228—
ProductHCID 178440106HCID 17844010664.4%

Reaction Steps

4-chloro-N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-2-propyl-1H-imidazole-5-carboxamide was prepared in a similar manner as described herein from 3-chloro-5-({6-chloro-2-fluoro-3-[(methylamino)methyl]phenyl}oxy)benzonitrile (0.062 g, 0.20 mmol), 4-chloro-2-propyl-1H-imidazole-5-carboxylic acid (0.038 g, 0.20 mmol), HATU (0.091 g, 0.24 mmol), DIPEA (0.042 mL, 0.24 mmol) and DMF (2 mL). Purification was accomplished by Reverse-Phase HPLC (water/acetonitrile with 0.1% TFA) to afford the title compound (0.062 g, 64%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 12.73 (br. s., 1H), 8.12 (br. s., 1H), 7.81-7.84 (m, 1H), 7.45-7.52 (m, 3H), 7.37 (t, 1H), 4.53 (d, 2H), 2.55 (t, 2H), 1.64 (sex, 2H), 0.87 (t, 3H). ES-LCMS: m/z 481.0, 483.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-4e3528c54f3346039fccdefede0b80c5
Source noteuspto-grants-2012_11