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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076207Generated: October 31, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 59140152, compound

https://huagongshe.com/reaction/2076207

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(2-(Vinyloxy)ethyl)hydroxylamineHCID 21867017—
ReactantHCID 59140183HCID 59140183—
SolventDimethylformamideHCID 6228—
ProductHCID 59140152HCID 5914015283.3%

Reaction Steps

8-Fluoro-5-(2-fluoro-4-iodo-phenylamino)-imidazo[1,5-a]pyridine-6-carboxylic acid (0.20 g, 0.48 mmol), O-(2-vinyloxyethyl)-hydroxylamine (55 mg, 0.53 mmol), EDCI (102 mg, 0.53 mmol), HOBt (72 mg, 0.53 mmol) and DIPEA (90 μL, 0.53 mmol) were dissolved in DMF (10 mL) and the reaction mixture stirred at room temperature for 16 hours before being concentrated in vacuo. The resultant residue was dissolved in ethyl acetate (10 mL), washed with aqueous saturated sodium bicarbonate solution (10 mL) and the aqueous fraction extracted twice with ethyl acetate (2×10 mL). The combined organic fractions were washed with brine (20 mL), dried (MgSO4) and concentrated in vacuo. The resultant residue was subjected to flash chromatography (SiO2, gradient 0-10% methanol in DCM) to yield the title compound as a pale yellow solid (200 mg, 83%). LCMS (Method B): RT=3.41 min, [M+H]+=501.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923456B2
Source datasetuspto-grants-2011_04
ORD IDord-f7333b87f2cd4846ac1511392abf052b
Source noteuspto-grants-2011_04