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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912214Generated: November 3, 2026

Methyl 4-bromobenzoate → HCID 67385537, compound

https://huagongshe.com/reaction/912214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-bromobenzoateHCID 12081—
Reactant4-((5-Bromopyridin-2-yl)carbonyl)morpholineHCID 26967019—
ReactantBis-(4-methoxybenzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amineHCID 45258862—
ProductHCID 67385537HCID 67385537—

Reaction Steps

Using 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 (5-bromo-pyridin-2-yl)-morpholin-4-yl-methanone (45 mg) obtained in the same manner as Step A in Example 1-D-79 instead of 4-bromobenzoic acid methyl ester in Example 1-D-08, in the same manner as Example 1-D-08, a crude product of [5-(4-{2-[bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidin-7-yl)-pyridin-2-yl]-morpholin-4-yl-methanone was obtained, and then the PMB groups were removed according to the above Deprotection method 1, to obtain the desired compound (D-85) as a colorless powder (37 mg, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-da7f5dc1a99a49dabacf92e3e0ed7016
Source noteuspto-grants-2011_09