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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912183Generated: November 1, 2026

4'-Bromoacetanilide → HCID 67386020, compound

https://huagongshe.com/reaction/912183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-BromoacetanilideHCID 7683—
ReactantMethyl 4-bromobenzoateHCID 12081—
ReactantCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
ReactantBis-(4-methoxybenzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amineHCID 45258862—
ReactantHCID 67386144HCID 67386144—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
ProductHCID 67386020HCID 67386020—

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 acetyl-(4-bromo-phenyl)-carbamic acid tert-butyl ester (prepared from N-(4-bromo-phenyl)-acetamide and di-t butyl carbonate in acetonitrile in the presence of DMAP, 94 mg) 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 acetyl-[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)-phenyl]-carbamic acid tert-butyl ester was obtained, and then the PMB groups were removed according to Deprotection method 1, to obtain the desired compound (D-43) as a pale yellow powder (7 mg, 17%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-669225557f194adc98dce2ab1c7fc8dc
Source noteuspto-grants-2011_09