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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912179Generated: November 3, 2026

HCID 67386071, compound → Bis-(4-methoxybenzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amine

https://huagongshe.com/reaction/912179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67386071HCID 67386071—
ReactantHCID 67386401HCID 67386401—
Solvent5-Bromo-2-fluoropyridineHCID 2783168—
ProductBis-(4-methoxybenzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amineHCID 45258862—

Reaction Steps

From bis-(4-methoxy-benzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amine (81 mg) and 2-fluoro-5-bromopyridine (30 μl), in the same manner as Step B in Example 1-D-25, crude products of {5-[7-(5-bromo-pyridin-2-yl)-2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl]-pyrimidin-2-yl}-bis-(4-methoxy-benzyl)-amine and {5-[7-(6-fluoro-pyridin-3-yl)-2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl]-pyrimidin-2-yl}-bis-(4-methoxy-benzyl)-amine were obtained, and then for each products the PMB groups were removed according to Deprotection method 3, to obtain the desired compound (D-36) as a colorless powder (5 mg, 32%) and as a colorless powder (D-37: 7 mg, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-b7f9cf4e9c4a4c48a7102afb801a1dd3
Source noteuspto-grants-2011_09