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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367916Generated: October 30, 2026

Diisopropylethylamine → HCID 58026467, compound

https://huagongshe.com/reaction/1367916

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 numberUS07893267B2
Source datasetuspto-grants-2011_02
ORD IDord-80a1bc1f3a0341958b20b6613699e7ee
Source noteuspto-grants-2011_02