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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069461Generated: October 30, 2026

Diisopropylethylamine → HCID 68510576, compound

https://huagongshe.com/reaction/2069461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantN-BOC-ethylenediamineHCID 187201—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 68508465HCID 68508465—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 68510576HCID 6851057680.2%

Reaction Steps

To a suspension of Intermediate 10 (25 mg, 0.061 mmol) in DMF is added DIPEA (16 μL, 0.092 mmol) followed by TBTU (23.5 mg, 0.073 mmol). The reaction mixture is stirred for 5 min before adding N-Boc-ethylenediamine (12 μL, 0.073 mmol) and stirring is continued for 2 h. The reaction mixture is diluted with EtOAc (20 mL) and is washed with sat. aq. NaHCO3 (15 mL). The org. phase is then dried over Na2SO4, filtered, and evaporated to give a yellow oil that is purified by prep. TLC (eluting with DCM/MeOH 95:5) to afford [2-(3-{2-ethyl-4-[5-(2-isopropylamino-6-methyl-pyrimidin-4-yl)-[1,2,4]oxadiazol-3-yl]-6-methyl-phenyl}-propionylamino)-ethyl]-carbamic acid tert-butyl ester (27 mg) as a white solid; LC-MS: tR=1.09 min; [M+1]+=552.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299086B2
Source datasetuspto-grants-2012_10
ORD IDord-b78714961f6b463ca28d5970fc64bbff
Source noteuspto-grants-2012_10