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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912219Generated: November 3, 2026

Methyl 4-bromobenzoate → HCID 67386257, compound

https://huagongshe.com/reaction/912219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-bromobenzoateHCID 12081—
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 62955059HCID 62955059—
ProductHCID 67386257HCID 67386257—

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 (100 mg) and (5-bromo-pyridin-2-yl)-(4-ethyl-piperazin-1-yl)-methanone (61 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, to obtain 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]-(4-ethyl-piperazin-1-yl)-methanone, and then the PMB groups were removed according to the above Deprotection method 1, to obtain the desired compound (D-95) as a milky white powder (52 mg, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-436caf533de744118ef7b2e04a959eea
Source noteuspto-grants-2011_09