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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912300Generated: 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 67385428, compound

https://huagongshe.com/reaction/912300

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—
Reactant1,1-Dimethylethyl 4-[(4-chloro-2-pyridinyl)carbonyl]-1-piperazinecarboxylateHCID 59244211—
ProductHCID 67385428HCID 6738542857.7%

Reaction Steps

Using 4-(4-chloro-pyridine-2-carbonyl)-piperazine-1-carboxylic acid tert-butyl ester (163 mg, 0.500 mmol) obtained in Step A instead of 4-chloropicolinic acid t-butylamide, and bis-(4-methoxy-benzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amine (245 mg, 445 mmol), in the same manner as Example 1-D-07, amination was carried out, to obtain a crude product of 4-[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)-pyridine-2-carbonyl]-piperazine-1-carboxylic acid tert-butyl ester as a yellow solid (239 mg), and further PMB group and BOC group were removed according to the above Deprotection method 2, to obtain the desired compound (D-199) as a yellow powder (67 mg, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-1cdfaec3cacc4b59827e0131bc10b100
Source noteuspto-grants-2011_09