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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092174Generated: November 1, 2026

Triethylamine → HCID 67236480, compound

https://huagongshe.com/reaction/2092174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Aminomethyl-1,4-benzodioxaneHCID 15053—
ReactantDiisopropylethylamineHCID 81531—
Reactantmethyl 4-({[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl}amino)-1H-indazole-1-carboxylateHCID 11313556—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67236480HCID 6723648092.2%

Reaction Steps

The product of Example 24D (635 mg, 1.9 mmol) was added to a solution of 1-(2,3-dihydro-1,4-benzodioxin-2-yl)methanamine (315 mg, 1.9 mmol) and diisopropylethylamine (0.34 mL, 1.9 mmol) in N,N-dimethylformamide (5 mL) under nitrogen atmosphere at ambient temperature. After 30 minutes the reaction solution was diluted with water (50 mL), the resulting precipitate was filtered off, washed with water and air-dried. The wet cake was added to a solution of methanol (25 mL), water (3 mL) and triethylamine (0.54 mL, 3.8 mmol). The mixture was refluxed for an hour, cooled to room temperature, diluted with water (100 mL), collected the white precipitate by filtration, rinsed with water and air-dried. The wet cake was vacuum dried to constant weight to provide the title compound (568 mg, 92%) as a white solid. 1H NMR (300 MHz, DMSO-d6) δ: 3.41-3.56 (m, 2H), 3.98 (dd, 1H), 4.26-4.33 (m, 1H), 4.36 (dd, 1H), 6.68 (t, 1H), 6.81-6.94 (m, 4H), 7.06 (d, 1H), 7.20 (t, 1H), 7.62 (d, 1H), 8.09 (s, 1H), 8.80 (s, 1H), 13.00 (s, 1H). MS (ESI) m/z: 325.1 (M+H)+; Anal. Calc'd for C17H16N4O3: C, 62.95; H, 4.97; N, 17.27. Found: C, 62.66; H, 4.83; N, 16.99.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440691B2
Source datasetuspto-grants-2013_05
ORD IDord-efa391d3648448d9970e5af72efd6ee5
Source noteuspto-grants-2013_05