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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250868Generated: October 31, 2026

Diisopropylethylamine → HCID 57033673, compound

https://huagongshe.com/reaction/1250868

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 69922482HCID 69922482—
SolventTetrahydrofuranHCID 8028—
Solvent1,4,5,6-Tetrahydropyrimidin-2-amineHCID 3287412—
ProductHCID 57033673HCID 57033673—

Reaction Steps

56 mg of 4-{4-[(2S)-2-tert-butoxycarbonyl-2-(4-trifluoromethylbenzenesulfonylamino)-ethyl]-phenoxy}-butyric acid were dissolved in tetrahydrofuran and 12.5 mg of 1,4,5,6-tetrahydropyrimidin-2-ylamine, 68 mg of diisopropylethylamine and 44 mg of HATU were added. The reaction mixture was stirred overnight, and the solvent was removed in vacuo. The residue was dissolved in dichloromethane and washed with saturated aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution. The organic phase was dried with sodium sulfate, filtered and the solvent was removed in vacuo. The residue was chromatographed on reversed-phase (C-18) silica gel eluting with a gradient of 10-90% acetonitrile in water. Yield 37.3 mg. MS (FAB+): m/e=613.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340679B1
Source datasetuspto-grants-2002_01
ORD IDord-88afa19c42ee4650b8c5a96022b8b6bb
Source noteuspto-grants-2002_01