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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099067Generated: November 1, 2026

Diisopropylethylamine → 4-{3-[1-(1,3-benzothiazol-6-yl)cyclopropyl][1,2,4]triazolo[4,3-b][1,2,4]triazin-6-yl}-N-{(1S)-1-[(dimethylamino)carbonyl]propyl}benzamide

https://huagongshe.com/reaction/1099067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant(2S)-2-amino-N,N-dimethylbutanamide hydrochlorideHCID 57517874—
Reactant4-{3-[1-(1,3-Benzothiazol-6-yl)cyclopropyl][1,2,4]triazolo[4,3-b][1,2,4]triazin-6-yl}benzoic acidHCID 66813054—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product4-{3-[1-(1,3-benzothiazol-6-yl)cyclopropyl][1,2,4]triazolo[4,3-b][1,2,4]triazin-6-yl}-N-{(1S)-1-[(dimethylamino)carbonyl]propyl}benzamideHCID 59216344—

Reaction Steps

N,N-Diisopropylethylamine (14 μL, 0.080 mmol) was added to a mixture of 4-{3-[1-(1,3-benzothiazol-6-yl)cyclopropyl][1,2,4]triazolo[4,3-b][1,2,4]triazin-6-yl}benzoic acid (11 mg, 0.026 mmol), (2S)-2-amino-N,N-dimethylbutanamide hydrochloride (5.8 mg, 0.034 mmol) and benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (14 mg, 0.032 mmol) in DMF (0.4 mL). The mixture was stirred at RT overnight. The residue was diluted with methanol, and purified by RP-HPLC (pH=10) to afford the desired product. Analytical LCMS: (M+H)+=527.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143251B2
Source datasetuspto-grants-2012_03
ORD IDord-7b94ca06ad3141809b55d0f70d9ddb66
Source noteuspto-grants-2012_03