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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912204Generated: November 2, 2026

N,N-Dimethylpiperidin-4-amine → HCID 67384948, compound

https://huagongshe.com/reaction/912204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Dimethylpiperidin-4-amineHCID 417391—
ReactantHCID 59244926HCID 59244926—
ProductHCID 67384948HCID 6738494885.5%

Reaction Steps

Using {5-[7-(6-chloro-pyridin-3-yl)-2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl]-pyrimidin-2-yl}-bis-(4-methoxy-benzyl)-amine (200 mg, 0.31 mmol) obtained in Step A in Example 1-D-48 and 4-dimethylaminopiperidine (59 mg, 0.46 mmol) instead of N,N,N′-trimethyl ethylenediamine, in the same manner as Example 1-D-48, amination was carried out, 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)-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl]-dimethyl-amine as a yellow solid (197 mg), and then the PMB groups were removed according to the above Deprotection method 2, to obtain the desired compound (D-73) as a yellow powder (32 mg, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-ae8dda9fad2342809284c8e656e3ac68
Source noteuspto-grants-2011_09