Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912317Generated: October 27, 2026

1-(2-Hydroxyethyl)piperazine → 4-(2-Amino-pyrimidin-5-yl)-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-carboxylic acid methyl-{3-[methyl-(2-morpholin-4-yl-ethyl)-amino]-phenyl}-amide

https://huagongshe.com/reaction/912317

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
ReactantMethyl(2-(morpholin-4-yl)ethyl)amineHCID 14979282—
Reactant4-{2-[Bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-carboxylic acid (3-bromo-phenyl)-methyl-amideHCID 59244962—
Reactant4-{2-[Bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-carboxylic acid {3-[methyl-(2-morpholin-4-yl-ethyl)-amino]-phenyl}-amideHCID 86640131—
Product4-(2-Amino-pyrimidin-5-yl)-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-carboxylic acid methyl-{3-[methyl-(2-morpholin-4-yl-ethyl)-amino]-phenyl}-amideHCID 5924433422%

Reaction Steps

Using 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 (3-bromo-phenyl)-methyl-amide (112 mg) and methyl-(2-morpholin-4-yl-ethyl)-amine (25.8 mg) obtained in Step A in Example 1-D-139 instead of 2-piperazin-1-yl-ethanol, in the same manner as Step C in Example 1-D-153, 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 {3-[methyl-(2-morpholin-4-yl-ethyl)-amino]-phenyl}-amide was obtained as a crude product. The PMB groups were removed according to Deprotection method 3, to obtain the desired compound (D-227) as a brown solid (18.6 mg, 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-1db9ad1d9ee84ffe8d688770d91eb2d6
Source noteuspto-grants-2011_09