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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912151Generated: October 30, 2026

Ammonium Chloride → HCID 59244477, compound

https://huagongshe.com/reaction/912151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant4-(4-{2-[Bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-yl)-benzoic acidHCID 59244887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59244477HCID 59244477—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-(4-{2-[bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidin-7-yl)-benzoic acid (30 mg, 0.0468 mmol) obtained in Example 1-D-09 in dimethylformamide (1 ml), Hunig's base (41 μl, 0.234 mmol), HOBt monohydrate (8.3 mg, 0.0468 mmol), WSC hydrochloride (17.6 mg, 0.0702 mmol) and ammonium chloride (5.0 mg, 0.0936 mmol) were added, followed by stirring at 80° C. for 3 hours. To this, water (5 ml) was added, and the solid was filtered off. To this, trifluoroacetic acid (1 ml) and concentrated sulfuric acid (2 drops) were added, followed by stirring at 40° C. for 3 hours. After concentration of TFA under reduced pressure, water was added, followed by neutralization with 1M aqueous sodium hydroxide solution. The solid was filtered, and subsequently suspended in dichloromethane/hexane=9/1, which was stirred at room temperature for 30 minutes, followed by filtering the solid, to obtain the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-4b4842e46ecf491e8048fd469e48d10c
Source noteuspto-grants-2011_09