Structure of 25077-25-2
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
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| CAS No. : | 25077-25-2 |
| Formula : | C6H9NO2 |
| M.W : | 127.14 |
| SMILES Code : | O=C(CCC1)N(C)C1=O |
| MDL No. : | MFCD01725031 |
| InChI Key : | VUYOLIKWIVQHBC-UHFFFAOYSA-N |
| Pubchem ID : | 161476 |
| GHS Pictogram: |
|
| Signal Word: | Warning |
| Hazard Statements: | H302-H315-H319-H335 |
| Precautionary Statements: | P261-P305+P351+P338 |
| Num. heavy atoms | 9 |
| Num. arom. heavy atoms | 0 |
| Fraction Csp3 | 0.67 |
| Num. rotatable bonds | 0 |
| Num. H-bond acceptors | 2.0 |
| Num. H-bond donors | 0.0 |
| Molar Refractivity | 36.05 |
| TPSA ? Topological Polar Surface Area: Calculated from |
37.38 Ų |
| Log Po/w (iLOGP)? iLOGP: in-house physics-based method implemented from |
1.39 |
| Log Po/w (XLOGP3)? XLOGP3: Atomistic and knowledge-based method calculated by |
-0.5 |
| Log Po/w (WLOGP)? WLOGP: Atomistic method implemented from |
-0.23 |
| Log Po/w (MLOGP)? MLOGP: Topological method implemented from |
0.3 |
| Log Po/w (SILICOS-IT)? SILICOS-IT: Hybrid fragmental/topological method calculated by |
0.76 |
| Consensus Log Po/w? Consensus Log Po/w: Average of all five predictions |
0.34 |
| Log S (ESOL):? ESOL: Topological method implemented from |
-0.31 |
| Solubility | 61.8 mg/ml ; 0.486 mol/l |
| Class? Solubility class: Log S scale |
Very soluble |
| Log S (Ali)? Ali: Topological method implemented from |
0.18 |
| Solubility | 194.0 mg/ml ; 1.52 mol/l |
| Class? Solubility class: Log S scale |
Highly soluble |
| Log S (SILICOS-IT)? SILICOS-IT: Fragmental method calculated by |
-0.73 |
| Solubility | 23.7 mg/ml ; 0.187 mol/l |
| Class? Solubility class: Log S scale |
Soluble |
| GI absorption? Gatrointestinal absorption: according to the white of the BOILED-Egg |
High |
| BBB permeant? BBB permeation: according to the yolk of the BOILED-Egg |
No |
| P-gp substrate? P-glycoprotein substrate: SVM model built on 1033 molecules (training set) |
No |
| CYP1A2 inhibitor? Cytochrome P450 1A2 inhibitor: SVM model built on 9145 molecules (training set) |
No |
| CYP2C19 inhibitor? Cytochrome P450 2C19 inhibitor: SVM model built on 9272 molecules (training set) |
No |
| CYP2C9 inhibitor? Cytochrome P450 2C9 inhibitor: SVM model built on 5940 molecules (training set) |
No |
| CYP2D6 inhibitor? Cytochrome P450 2D6 inhibitor: SVM model built on 3664 molecules (training set) |
No |
| CYP3A4 inhibitor? Cytochrome P450 3A4 inhibitor: SVM model built on 7518 molecules (training set) |
No |
| Log Kp (skin permeation)? Skin permeation: QSPR model implemented from |
-7.43 cm/s |
| Lipinski? Lipinski (Pfizer) filter: implemented from |
0.0 |
| Ghose? Ghose filter: implemented from |
None |
| Veber? Veber (GSK) filter: implemented from |
0.0 |
| Egan? Egan (Pharmacia) filter: implemented from |
0.0 |
| Muegge? Muegge (Bayer) filter: implemented from |
1.0 |
| Bioavailability Score? Abbott Bioavailability Score: Probability of F > 10% in rat |
0.55 |
| PAINS? Pan Assay Interference Structures: implemented from |
0.0 alert |
| Brenk? Structural Alert: implemented from |
1.0 alert: heavy_metal |
| Leadlikeness? Leadlikeness: implemented from |
No; 1 violation:MW<1.0 |
| Synthetic accessibility? Synthetic accessibility score: from 1 (very easy) to 10 (very difficult) |
1.0 |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

[ 25077-25-2 ]
[ 110-83-8 ]
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 56% | With silver tetrafluoroborate; water; Selectfluor; In acetone; at 40℃; for 1h;Schlenk technique; Inert atmosphere; | General procedure: To a 1-dram vial was added sequentially 1a (18.9 mg, 0.100 mmol), AgBF4 (77.9 mg, 0.400 mmol), Selectfluor (142 mg, 0.400 mmol) and 1 :9 acetone: H20 (0.5 mL) The resulting mixture was heated to 40 C and held at this temperature. After 1 h, the reaction mixture was partitioned with EtOAc (0.5 mL) and H20 (0.5 mL) and the phases were separated. The aqueous phase was extracted with EtOAc (1.5 mL c 3) and the combined organic layers were concentrated under reduced pressure. The crude residue was purified by preparative thin-layer chromatography (50% EtO Ac/hexanes) to provide A-(4-fl uorobutyl )- A'-form yl benzam i de (2a) (18.0 mg, 81%) as a pale yellow oil. NMR (600 MHz, CDCh): d 8.93 (s, 1H), 7.57 (t, J= 7.2 Hz, 1H), 7.53-7.48 (m, 4H), 4.48 (dt, J= 47.6, 5.6 Hz, 2H), 3.92 (t, J= 7.1 Hz, 2H), 1.82-1.72 (m, 4H); 13C NMR (151 MHz, CDCh): 172.5, 164.3, 133.7, 132.3, 129.1, 128.9, 83.6 (d, J = 165.2 Hz), 40.2, 28.0 (d, J= 20.2 Hz), 24.2 (d, J= 5.0 Hz); 19F NMR (376 MHz, CDCh): d -217.5 - -217.9 (m, 1F); HRMS (ESI): Calc?d for Ci2Hi4FN02Na [M+Na]+: 246.0906, found: 246.0906. |

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