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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44428Generated: October 25, 2026

Acefylline → HCID 45254481, compound

https://huagongshe.com/reaction/44428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcefyllineHCID 69550—
Reactant2-(4-Aminophenyl)propan-2-olHCID 9543261—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventN,N-dimethylformamide; methylsulfinylmethaneHCID 3013483—
ProductHCID 45254481HCID 45254481—

Reaction Steps

To a 0° C. solution of acid 101 (0.32 g, 1.34 mmol) in DMF/DMSO (1:1, 20 mL) was added HATU (0.0.76 g, 2.01 mmol). The reaction was then stirred an additional 15 min at room temperature. The solution was cooled to 0° C. and amine 135 (0.30 g, 2.01 mmol) was added. The reaction was then stirred at rt overnight. The DMF was concentrated in vacuo and water was added to the reaction. The aqueous layer was extracted with EtOAc The ethyl acetate layer was then washed again with water and the organic layer was concentrated in vacuo. The product was purified by flash chromatography on silica gel eluting with EtOAc/hexanes and EtOAc/MeOH to yield 402 as a pure light brown semi solid (0.086 g, 17.5%). MS (APCI): m/z 372.2 [M−H]+ Anal. Calcd. For C18H21N5O4. 0.35 EtOAc: C, 57.93; H, 5.96; N, 17.41. Found C, 58.36; H, 6.14; N, 16.96.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541423B2
Source datasetuspto-grants-2013_09
ORD IDord-baba062cb47f4c34aaf02c30011c1cd1
Source noteuspto-grants-2013_09