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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77171Generated: October 30, 2026

4-Methylmorpholine → HCID 53495394, compound

https://huagongshe.com/reaction/77171

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant3-Amino-1-propanolHCID 9086—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-Hydroxy-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetic acidHCID 67458957—
SolventDimethylformamideHCID 6228—
ProductHCID 53495394HCID 5349539426.5%

Reaction Steps

(R/S)-2-Hydroxy-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetic acid (Int-V, 30 mg, 0.070 mmol), 3-aminopropan-1-ol (7.84 mg, 0.104 mmol), 4-methylmorpholine (28.1 mg, 0.278 mmol), and HATU (34.4 mg, 0.090 mmol) were dissolved in DMF (1 mL). The mixture was stirred for 1 h and then purified by prep HPLC (PHENOMENEX® Luna 5u 21×250 mm, gradient elution with Method 1—MeOH/water containing 0.1% trifluoroacetic acid as defined above, 0% B to 100% B over 30 min, 25 mL/min, 220 nM, product retention=29.4 min) to provide (R/S)-2-hydroxy-N-(3-hydroxypropyl)-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide (12 mg, 0.018 mmol, 26.5% yield): LCMS=489.1 [M+H]+; 1H NMR (400 MHz, chloroform-d) δ ppm 8.12-8.30 (2 H, m), 7.47-7.74 (7 H, m), 7.06 (1 H, br. s.), 5.22 (1 H, d, J=4.83 Hz), 4.38 (1 H, t, J=5.71 Hz), 3.56-3.75 (2 H, m), 3.31-3.52 (2 H, m), 1.91-2.08 (1 H, m), 1.63-1.81 (2 H, m); HPLC peak RT=8.4 min (Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835470B2
Source datasetuspto-grants-2014_09
ORD IDord-0e521cbae03b4a3dbb0c7ef66f04aa34
Source noteuspto-grants-2014_09