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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500723Generated: November 2, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 59140134, compound

https://huagongshe.com/reaction/1500723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-(+)-2,2-Dimethyl-4-hydroxyaminomethyl-1,3-dioxolaneHCID 23541087—
ReactantHCID 59140183HCID 59140183—
SolventDimethylformamideHCID 6228—
ProductHCID 59140134HCID 5914013497%

Reaction Steps

8-Fluoro-5-(2-fluoro-4-iodo-phenylamino)-imidazo[1,5-a]pyridine-6-carboxylic acid (235 mg, 0.57 mmol), O—(((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-hydroxylamine (92 mg, 0.62 mmol), EDCI (120 mg, 0.62 mmol), HOBt (84 mg, 0.62 mmol) and DIPEA (0.1 mL, 0.62 mmol) were dissolved in DMF (10 mL) and the reaction mixture stirred at room temperature for 72 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 with 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 (298 mg, 97%). LCMS (Method B): RT=3.34 min, [M+H]+=545.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206174B2
Source datasetuspto-grants-2015_12
ORD IDord-f81c2616f9f04a3380166e62bfda4cf7
Source noteuspto-grants-2015_12