Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250865Generated: October 30, 2026

Diisopropylethylamine → HCID 57276081, compound

https://huagongshe.com/reaction/1250865

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 57041896HCID 57041896—
SolventTetrahydrofuranHCID 8028—
Solvent1,4,5,6-Tetrahydropyrimidin-2-amineHCID 3287412—
ProductHCID 57276081HCID 57276081—

Reaction Steps

88 mg of 4-[4-((2S)-2-benzenesulfonylamino-2-tert-butoxycarbonyl-ethyl)-phenoxy]-butyric acid were dissolved in tetrahydrofuran and 22.6 mg of 1,4,5,6-tetrahydropyrimidin-2-ylamine, 123 mg of diisopropylethylamine and 79.4 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-1 8) silica gel eluting with a gradient of 10-90% acetonitrile in water. Yield 40.1 mg. MS (FAB+): m/e=545.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340679B1
Source datasetuspto-grants-2002_01
ORD IDord-90f4e60d88af4e47851ef3ccb2fb27f0
Source noteuspto-grants-2002_01