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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910259Generated: October 28, 2026

Diisopropylethylamine → (5-Butyl-1-(5-methyl-4-(thiophen-2-yl)pyrimidin-2-yl)-1H-pyrazol-4-yl)(5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone

https://huagongshe.com/reaction/910259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant5H,6H,7H,8H-(1,2,4)triazolo(4,3-a)pyrazineHCID 17998718—
ReactantHCID 60207815HCID 60207815—
SolventDimethylformamideHCID 6228—
Product(5-Butyl-1-(5-methyl-4-(thiophen-2-yl)pyrimidin-2-yl)-1H-pyrazol-4-yl)(5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanoneHCID 673904533.2%

Reaction Steps

To a solution of 5-butyl-1-(5-methyl-4-(thiazol-5-yl)pyrimidin-2-yl)-1H-pyrazole-4-carboxylic acid (72 mg, 0.21 mmol), 5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine (50 mg, 0.23 mmol), HBTU (119 mg, 0.32 mmol) and 4 mL of DMF was added DIEA (54 μL, 0.73 mmol). The reaction was stirred at room temperature for 2 hours at which time the crude mixture was purified directly by reverse phase preparative HPLC to provide 3.0 mg of 30 as a white solid. 1H NMR (400 MHz, MeOD-d3) δ 0.78 (t, J=7.2 Hz, 3H), 1.35 (m, 2H), 1.61 (m, 2 H), 2.69 (s, 3H), 3.4 (t, J=7.7 Hz, 2H), 4.18 (t, J=5.1 Hz, 2H), 4.31 (t, J=5.5 Hz, 2H), 5.10 (s, 2H), 7.32 (t, J=4.5 Hz, 1H), 7.82 (d, J=5.1 Hz, 1H), 7.96 (s, 1H), 7.99 (d, J=2.7 Hz, 1H), 8.54 (s, 1H), 8.76 (s, 1H). LCMS (ES+) m/z 449 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022061B2
Source datasetuspto-grants-2011_09
ORD IDord-457f18792aa04102aa5d4f06cd645031
Source noteuspto-grants-2011_09