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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435031Generated: November 4, 2026

(4-Chloro-pyrimidin-2-yl)(2,2,6,6-tetramethyl-piperidin-4-yl)-amine → HCID 57936296, compound

https://huagongshe.com/reaction/1435031

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chloro-pyrimidin-2-yl)(2,2,6,6-tetramethyl-piperidin-4-yl)-amineHCID 57936167—
ReactantHCID 69061243HCID 69061243—
ProductHCID 57936296HCID 57936296—

Reaction Steps

The title compound was prepared as described in Example 215, starting from {2-[1-(tert-butyl-dimethyl-silanyl)-1H-indol-6-yl]-1-methyl-ethyl}-trityl-amine (prepared by trityl and TBDMS protection of 2-(1H-Indol-6-yl)-1-methyl-ethylamine) and (4-chloro-pyrimidin-2-yl)-(2,2,6,6-tetramethyl-piperidin-4-yl)-amine, followed by in situ removal of the protecting groups with 2N-HCl. Yield: 406 mg (31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615562B2
Source datasetuspto-grants-2009_11
ORD IDord-b1e73572c6154c068a9bedb44a63ca24
Source noteuspto-grants-2009_11