Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353472Generated: October 31, 2026

Methylamine → 4-(2-Amino-7-chloro-4-quinolinyl)-N-[3-[(methylamino)carbonyl]cyclohexyl]-1-piperazinecarboxamide

https://huagongshe.com/reaction/1353472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
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—
Reactant3-[[[4-(2-Amino-7-chloro-4-quinolinyl)-1-piperazinyl]carbonyl]amino]cyclohexanecarboxylic acidHCID 21101592—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-(2-Amino-7-chloro-4-quinolinyl)-N-[3-[(methylamino)carbonyl]cyclohexyl]-1-piperazinecarboxamideHCID 21101675—

Reaction Steps

The mixture of 3-[[[4-(2-amino-7-chloro-4-quinolinyl)-1-piperazinyl]carbonyl]amino]cyclohexanecarboxylic acid (30 mg, 0.069 mmol), HATU (100 mg), methylamine (1.0M in THF, 3 mL) and diisopropylethylamine (0.5 mL) in DMF (3 mL) was stirred at rt for 3 h. The reaction mixture was diluted with ethyl acetate (100 mL), washed with sat. NaHCO3 solution and water, and dried over Na2SO4. Concentration in vacuo followed by flash chromatography afforded the title product. LC-MS: 445 (M++1). 1H NMR (CD3OD) δ 1.10–1.35 (m, 4H), 1.65–1.90 (m, 4H), 2.20 (m, 1H), 2.65 (s, 3H), 3.08 (m, 4H), 3.60 (m, 5H), 5.80 (d, 1H), 6.15 (s, 1H), 7.10 (d, 2H), 7.45 (s, 1H), 7.65 (a, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220856B2
Source datasetuspto-grants-2007_05
ORD IDord-575462f61af24223b90996cd8e5be682
Source noteuspto-grants-2007_05