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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912338Generated: November 3, 2026

4-((5-Bromopyridin-3-yl)sulfonyl)morpholine → HCID 67385766, compound

https://huagongshe.com/reaction/912338

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((5-Bromopyridin-3-yl)sulfonyl)morpholineHCID 25307198—
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 67385766HCID 67385766—

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 4-(5-bromo-pyridine-3-sulfonyl)-morpholine (prepared from 5-bromo-pyridine-3-sulfonyl chloride and morpholine, 60 mg) instead of 4-bromobenzoic acid methyl ester used in Example 1-D-8, in the same manner as Example 1-D-07, a crude product of bis-(4-methoxy-benzyl)-(5-{7-[5-(morpholine-4-sulfonyl)-pyridin-3-yl]-2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl}-pyrimidin-2-yl)-amine was obtained, and then the PMB groups were removed according to the above Deprotection method 3, to obtain the desired compound (D-248) as an ivory powder (65 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-9873fc1377e04ba38c3b0171e0b8eef5
Source noteuspto-grants-2011_09