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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775304Generated: November 1, 2026

3,3-Diethoxypropyne → tert-butyl N-[2-[[2-chloro-5-(3,3-diethoxyprop-1-ynyl)pyrimidin-4-yl]amino]-2-methyl-propyl]carbamate

https://huagongshe.com/reaction/1775304

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-DiethoxypropyneHCID 66285—
Reactanttert-butyl N-[2-[[2-chloro-5-(3,3-diethoxyprop-1-ynyl)pyrimidin-4-yl]amino]ethyl]carbamateHCID 86695595—
Reactanttert-butyl N-[2-[(5-bromo-2-chloro-pyrimidin-4-yl)amino]-2-methyl-propyl]carbamateHCID 86695601—
Producttert-butyl N-[2-[[2-chloro-5-(3,3-diethoxyprop-1-ynyl)pyrimidin-4-yl]amino]-2-methyl-propyl]carbamateHCID 89789736—

Reaction Steps

tert-butyl N-[2-[[2-chloro-5-(3,3-diethoxyprop-1-ynyl)pyrimidin-4-yl]amino]-2-methyl-propyl]carbamate is synthesized by treating tert-butyl N-[2-[(5-bromo-2-chloro-pyrimidin-4-yl)amino]-2-methyl-propyl]carbamate with 3,3-diethoxyprop-1-yne in the presence of a catalyst such as Pddba using similar experimental conditions as described for the synthesis of tert-butyl N-[2-[[2-chloro-5-(3,3-diethoxyprop-1-ynyl)pyrimidin-4 yl]amino]ethyl]carbamate LCMS (ESI) (M+H) 427.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260442B2
Source datasetuspto-grants-2016_02
ORD IDord-dbddc203afa84fada27d93c1550d234e
Source noteuspto-grants-2016_02