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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470342Generated: October 30, 2026

4-Methylmorpholine → HCID 56848566, compound

https://huagongshe.com/reaction/1470342

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant2-Amino-2-methyl-1-propanolHCID 11807—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 66778978HCID 66778978—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 56848566HCID 5684856642%

Reaction Steps

3-Methyl-5-(7-phenyl-furo[3,2-b]pyridin-2-yl)-benzoic acid (79 μmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimidhydrochlorid (86,592 μmol) are dissolved in N,N-dimethylformamid (300.00 μl) and 4-methylmorpholin (157.354 μmol) and 1-hydroxybenzotriazolhydrat (86.849 μmol) are added and stirred 5 min at RT. A solution of 2-amino-2-methyl-propan-1-ol (80,000 μmol) in N,N-dimethylformamid (100.00 μl) is added. The mixture is stirred 4.5 h at RT. The reaction solution is poured into water and extracted with ethylacetate. The combined organic layers are dried over MgSO4 and the solvent is removed in vacuo. The product is isolated after reversed phase column chromatography as yellow solid (33 μmol, 42% yield). HPLC (method A): Rt 2.55 min (purity 98.5%); LCMS (ESI+) (method E): Rt 2.199 min, M+H+401.1 m/z; 1H NMR (500 MHz, DMSO-d6) δ [ppm] 8.60 (d, J=5.1, 1H), 8.18 (s, 1H), 8.16-8.10 (m, 2H), 7.96 (s, 1H), 7.77 (s, 1H), 7.70 (d, J=8.9, 2H), 7.65 (dd, J=14.7, 6.4, 3H), 7.58 (d, J=7.4, 1H), 4.16 (br, 1H), 3.54 (s, 2H), 2.47 (s, 3H), 1.35 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006440B2
Source datasetuspto-grants-2015_04
ORD IDord-aa5e00a369754f06a093588d765f54d1
Source noteuspto-grants-2015_04