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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910942Generated: November 2, 2026

Triethylamine → HCID 87076695, compound

https://huagongshe.com/reaction/910942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
ReactantHCID 24825978HCID 24825978—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87076695HCID 8707669582.3%

Reaction Steps

Using the method of Example 32, 2-(2-(4-methylthiazol-2-ylamino)pyridin-4-yloxy)benzoic acid (0.1 g, 0.3055 mmol), triethylamine (0.2129 mL, 1.527 mmol), ethyl carbonochloridate (0.03213 mL, 0.3360 mmol), N,N,N-trimethylethylenediamine (0.1191 mL, 0.9164 mmol) in THF (2 mL) were reacted to provide N-(2-(dimethyl-amino)ethyl)-N-methyl-2-(2-(4-methylthiazol-2-ylamino)pyridin-4-yloxy)benzamide dihydrochloride (0.067 g, 44.82% yield) as off white solid. 1H NMR (CDCl3) δ 8.20 (d, 1H), 7.57 (d, 1H), 7.50 (t, 1H), 7.38 (t, 1H), 7.13 (d, 1H), 6.79 (s, 1H), 6.59 (dd, 1H), 6.40 (d, 1H), 3.97 (m, 2H), 3.17 (m, 2H), 3.03 (s, 3H), 2.87 (s, 6H), 2.41 (s, 3H); Mass spectrum (esi) m/z=412 (100) (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022222B2
Source datasetuspto-grants-2011_09
ORD IDord-9fba864dcb5243a29fffd17c6cfba673
Source noteuspto-grants-2011_09