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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912350Generated: November 2, 2026

(4-Bromo-3-methylphenyl)(pyrrolidin-1-yl)methanone → HCID 67385437, compound

https://huagongshe.com/reaction/912350

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Bromo-3-methylphenyl)(pyrrolidin-1-yl)methanoneHCID 18960561—
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 67385437HCID 67385437—

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 (50 mg) and (4-bromo-3-methyl-phenyl)-pyrrolidin-1-yl-methanone (38 mg) instead of 4-chloropicolinic acid t-butylamide, in the same manner as Example 1-D-07, 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-methyl-phenyl]-pyrrolidin-1-yl-methanone was obtained, and then the PMB groups were removed according to the above Deprotection method 3, to obtain the desired compound (D-267) as a pale yellow powder (7 mg, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-9f63b56d080847f78ea45fad9bc3a90a
Source noteuspto-grants-2011_09