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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441363Generated: November 5, 2026

Triethylamine → HCID 178454300, compound

https://huagongshe.com/reaction/1441363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 45088832HCID 45088832—
Reactanttert-butyl (NZ)-N-[[(2-methylpropan-2-yl)oxycarbonylamino]-(trifluoromethylsulfonyl)methylidene]carbamateHCID 87540273—
SolventDichloromethaneHCID 6344—
ProductHCID 178454300HCID 17845430083%

Reaction Steps

To a solution of {[(Z)-tert-butoxycarbonylimino]-trifluoromethanesulfonyl-methyl}-carbamic acid tert-butyl ester (13.62 g, 34.8 mM) and triethylamine (4.9 ml, 34.8 mM) in dry DCM (183 ml), 1-(4-aminophenyl)azetidin-3-ol (Method 37; 6.0 g, 36.5 mM) was added. The solution was stirred at room temperature under nitrogen for 48 hours. The reaction mixture was diluted with more DCM and washed with water (twice), saturated sodium bicarbonate solution (twice), water and saturated sodium chloride. The solution was then dried with anhydrous sodium sulphate, filtered and evaporated. The crude product was triturated with ether/isohexane (2:1), filtered washed with the same solvent and dried to give the title compound as a yellow solid (11.77 g, 83%). NMR 1.4 (s, 9H), 1.5 (s, 9H), 3.47 (t, 1H), 4.02 (t, 2H), 4.5 (m, 1H), 5.55 (d, 1H), 6.38 (d, 2H), 7.23 (d, 2H), 9.75 (s, 1H), 11.46 (m, 1H); m/z 407.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655652B2
Source datasetuspto-grants-2010_02
ORD IDord-c48bc523271e470f9baf2d552585fea4
Source noteuspto-grants-2010_02