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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912222Generated: November 1, 2026

Methyl 4-bromobenzoate → HCID 67385716, compound

https://huagongshe.com/reaction/912222

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 67384979HCID 67384979—
ProductHCID 67385716HCID 67385716—

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 (120 mg) and 4-bromo-N-Boc-N-(3-hydroxy-propyl)-benzenesulfonamide (105 mg) obtained in the same manner as Example 1-D-80 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 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)-N-(3-hydroxy-propyl)-benzenesulfonamide was obtained, and then the PMB groups were removed according to the above Deprotection method 1, to obtain the desired compound (D-98) as a yellow powder (19 mg, 17%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-63f53e93218742e28c4bcb22c7d405a7
Source noteuspto-grants-2011_09