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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912178Generated: October 30, 2026

Ammonium Chloride → 4-{2-[Bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-carboxylic acid (2-carbamoyl-ethyl)-amide

https://huagongshe.com/reaction/912178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-[(4-{2-[Bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-carbonyl)-amino]-propionic acidHCID 59244610—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-{2-[Bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-carboxylic acid (2-carbamoyl-ethyl)-amideHCID 5924469284%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a DMF solution (1 ml) of 3-[(4-{2-[bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-carbonyl)-amino]-propionic acid (40 mg) obtained in Step A, ammonium chloride (6.5 mg), N-ethyldiisopropylamine (53 μl), HOBt (8.3 mg) and WSCI (17.6 mg) were added, followed by stirring at 80° C. for 3 hours. To this, water was added and the resulting solid was filtered, to obtain a crude product of the desired compound (33.5 mg, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-f8b2bda0bece47f2af582553464ed0a7
Source noteuspto-grants-2011_09