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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530516Generated: October 28, 2026

Triethylamine → HCID 73356786, compound

https://huagongshe.com/reaction/530516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 73291991HCID 73291991—
SolventDichloromethaneHCID 6344—
ProductHCID 73356786HCID 7335678639.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under nitrogen atmosphere at 0° C., to a stirred mixture of (2R,3S)-2-(5-cyclohexylpentoxycarbonylamino)-3-hydroxy-butanoic acid (0.32 g, 1.02 mmol) in dry CH2Cl2 (30 mL), Et3N (0.43 mL, 3.08 mmol) and subsequently TBTU (0.39 g, 1.2 mmol) were added. The mixture was left stirring 1 h at 0° C. and 15 h rt. Upon full conversion of the starting material, the organics were removed under reduced pressure, and the resulting crude product absorbed over silica gel and purified by typical column chromatography, eluting with Cy/AcOEt (from 100:0 to 0:100) to afford the title compound (0.12 g, 39%) as white solid. MS (ESI) m/z: 298 [M−H]+; (ESI) m/z: 296 [M−H]−. 1H NMR: δ 0.78-0.93 (m, 2H), 1.05-1.33 (m, 10H), 1.36 (d, J=6.4 Hz, 3H), 1.51-1.72 (m, 7H), 3.92-4.09 (m, 2H), 4.86 (dq, J=6.3 Hz, 1H), 5.42 (dd, J=6.1, 9.4 Hz, 1H), 8.20 (d, J=9.4 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353075B2
Source datasetuspto-grants-2016_05
ORD IDord-00a8afd7b8c944ec8656a402e06e25d3
Source noteuspto-grants-2016_05