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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362318Generated: November 1, 2026

Diisopropylethylamine → HCID 71293426, compound

https://huagongshe.com/reaction/2362318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 71293468HCID 71293468—
SolventDimethylformamideHCID 6228—
ProductHCID 71293426HCID 7129342654.3%

Reaction Steps

Intermediate 17 (50 mg, 0.10 mmol) was dissolved in DMF (1 mL). and diisopropylethylamine (50 μL, 0.29 mmol) and HATU (41 mg, 0.11 mmol) were added. The reaction mixture was stirred at RT for 30 minutes, then N,N,N-trimethylbutanediamine (38 mg, 0.29 mmol) was added, and stirring was continued for a further 18 hours. The reaction mixture was partitioned between EtOAc and water. The organic layer was separated, and the aqueous layer further extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4) and evaporated in vacuo. The resulting residue was purified by silica gel chromatography eluting with a gradient of 0-10% (2M NH3 in MeOH) in DCM to yield the title compound as a white solid (34 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691826B2
Source datasetuspto-grants-2014_04
ORD IDord-21ce532641b44c0d9efbc9fea45ecc3d
Source noteuspto-grants-2014_04