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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912361Generated: November 2, 2026

1-(2-Pyridyl)piperazine → HCID 67385809, compound

https://huagongshe.com/reaction/912361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Pyridyl)piperazineHCID 94459—
Reactant4-(4-{2-[Bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidin-7-yl)-3-fluoro-benzoic acidHCID 59244395—
ProductHCID 67385809HCID 67385809143.1%

Reaction Steps

Using 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)-3-fluoro-benzoic acid (80.0 mg, 0.118 mmol) obtained in Step A in Example 1-D-21 and 1-(2-pyridyl)piperazine (38.5 mg, 0.236 mmol) instead of 1-pyridine-3-yl-piperazine, amidation was carried out in the same manner as Step B in Example 1-D-21, to obtain a crude product 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]-3-fluoro-phenyl}-(4-pyridin-2-yl-piperazin-1-yl)-methanone as a yellow solid (139 mg), and then the PMB groups were removed according to the above Deprotection method 3, to obtain the desired compound (D-285) as a yellow powder (54.8 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-43729125f5ef4c78a6183ed310bb3ae3
Source noteuspto-grants-2011_09