Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520760Generated: November 4, 2026

4-Methylmorpholine → HCID 178452470, compound

https://huagongshe.com/reaction/1520760

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantPyrazole-5-carboxylic acid, 3-phenyl-HCID 121025—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant(S)-Tert-butyl 2-(4-aminophenyl)morpholine-4-carboxylateHCID 66705988—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178452470HCID 17845247074.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

In a 25 mL round-bottomed flask, (S)-tert-butyl 2-(4-aminophenyl)morpholine-4-carboxylate (100 mg, 359 μmol, Eq: 1.00), 3-phenyl-1H-pyrazole-5-carboxylic acid (87.9 mg, 467 μmol, Eq: 1.3) (CAS-1134-49-2), N-Methylmorpholine (109 mg, 118 μl, 1.08 mmol, Eq: 3) and HBTU (204 mg, 539 μmol, Eq: 1.5) were combined with DMF (3.75 ml). The reaction mixture was stirred at 60° C. for 16.5 hours. The mixture was poured into water (10 ml) and extracted twice with EtOAc. The organic layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified by column chromatography. (6 g silica gel (63-200A), eluent: heptane/EtOAc 2:1) to give the title compound as a white solid (120 mg, 74.5%). MS (ISP): 449.5 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073911B2
Source datasetuspto-grants-2015_07
ORD IDord-919672a21cf345c6936d7ad14722f433
Source noteuspto-grants-2015_07