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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910187Generated: October 31, 2026

Diisopropylethylamine → HCID 58026467, compound

https://huagongshe.com/reaction/1910187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant5-(Benzyloxy)pyridine-3-carboxylic acidHCID 18422069—
ReactantHCID 178508178HCID 178508178—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58026467HCID 5802646711%

Reaction Conditions

Temperature80 °C

Reaction Steps

0.07 g (0.30 mmol) of 5-benzyloxy-nicotinic acid and 0.12 g (0.32 mmol) of HBTU were combined in a flask charged with 2 mL DMF and 0.25 mL of DIEA. This reaction mixture was then treated with 0.05 g (0.20 mmol) of 2-Amino-3H-benzoimidazole-4-carboxylic acid (1H-imidazol-2-yl)-amide (Intermediate B) and stirred at 80° C. for 1 h. The reaction mixture was diluted with water, and the resultant solid precipitate was filtered and washed with saturated NaHCO3. The solid was dissolved with MeOH, evaporated onto silica gel and isolated by flash column chromatography (500 mL DCM/20 mL NH3/MeOH) to yield 10 mg (10%) of 2-[(5-benzyloxy-pyridine-3-carbonyl)-amino]-1H-benzoimidazole-4-carboxylic acid (1H-imidazol-2-yl)-amide. LCMS: 455.0 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598353B2
Source datasetuspto-grants-2013_12
ORD IDord-75efe6ff7e5f46fd8fadc4e7fbee5fb6
Source noteuspto-grants-2013_12