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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333703Generated: October 30, 2026

Triethylamine → Isobutyl 1-(2-(2-methoxyphenyl)thieno[3,2-d]pyrimidin-4-yl)piperidin-4-ylcarbamate

https://huagongshe.com/reaction/333703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl piperidin-4-ylcarbamateHCID 15676964—
Reactant4-Chloro-2-(2-methoxyphenyl)thieno[3,2-d]pyrimidineHCID 59026633—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductIsobutyl 1-(2-(2-methoxyphenyl)thieno[3,2-d]pyrimidin-4-yl)piperidin-4-ylcarbamateHCID 5902663455%

Reaction Steps

A solution of 4-chloro-2-(2-methoxyphenyl)thieno[3,2-d]pyrimidine (0.15 g, 0.54 mmol), isobutyl piperidin-4-ylcarbamate (0.11 g, 0.54 mmol), and Et3N (0.15 mL, 1.1 mmol) in DMF (1.8 mL) was heated in a microwave oven at 180° C. for 5 min. The reaction was cooled and diluted with CH2Cl2. The solution was washed with water, dried over Na2SO4, and concentrated under vacuum to give isobutyl 1-(2-(2-methoxyphenyl)thieno[3,2-d]pyrimidin-4-yl)piperidin-4-ylcarbamate (0.13 g, 55% yield). LC/MS: m/z 441.5 (M+H)+ at 2.55 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883781B2
Source datasetuspto-grants-2014_11
ORD IDord-781132a894854dd6a92da1932960f9c7
Source noteuspto-grants-2014_11