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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912308Generated: November 1, 2026

Bis-(4-methoxybenzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amine → HCID 67385778, compound

https://huagongshe.com/reaction/912308

Reaction equation

Participants

RoleNameHCIDCharge
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 67386297HCID 67386297—
ProductHCID 67385778HCID 67385778—

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-bromo-3,N-dimethyl-N-(2-morpholin-4-yl-ethyl)-benzamide (114 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,N-dimethyl-N-(2-morpholin-4-yl-ethyl)-benzamide was obtained, and further PMB group was removed according to the above Deprotection method 3, to obtain the desired compound (D-205) as a brown oil (68 mg, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-02562bb5324b41b6a6d0a7817e4bcf67
Source noteuspto-grants-2011_09