Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220406Generated: October 30, 2026

Hydrochloric Acid → HCID 67059656, compound

https://huagongshe.com/reaction/220406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMorpholineHCID 8083—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86651856HCID 86651856—
SolventMethanolHCID 887—
ProductHCID 67059656HCID 6705965655.1%

Reaction Steps

To a stirred solution of N,N-dicyclopropyl-6-ethyl-4-(5-formyl-1-methyl-1H-pyrazol-3-ylamino)-1-methyl-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide (example 112B, 22 mg, 0.049 mmol) and molecular seives 4 Å (30 mg) in MeOH (2 mL) was added morpholine (0.017 mL, 0.197 mmol). After the solution was stirred at room temperature for 12 hrs, sodium borohydride (7.46 mg, 0.197 mmol) was then added and stirred for 3 hrs. The solution was brought to pH=4 with 1N HCl, neutralized with saturated aqueous sodium bicarbonate, and then extracted with CH2Cl2. The organic layer was dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was purified by silica-gel flash chromatography using an Isco 40 g column eluting from 0-10% MeOH/CH2Cl2 to yield N,N-dicyclopropyl-6-ethyl-1-methyl-4-(1-methyl-5-(morpholinomethyl)-1H-pyrazol-3-ylamino)-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridine-7-carboxamide (14.3 mg, 0.027 mmol, 54.9% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202881B2
Source datasetuspto-grants-2012_06
ORD IDord-3df7ec06d966440ea6655a1ae8faa144
Source noteuspto-grants-2012_06