Structure of 187949-86-6
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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. : | 187949-86-6 |
Formula : | C11H8ClNO2S |
M.W : | 253.70 |
SMILES Code : | NC1=C(SC(=C1)C2=CC=C(C=C2)Cl)C(=O)O |
MDL No. : | MFCD09909681 |
InChI Key : | HTTXGCKIKMLVMR-UHFFFAOYSA-N |
Pubchem ID : | 10538839 |
GHS Pictogram: |
![]() |
Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H332-H335 |
Precautionary Statements: | P261-P280-P305+P351+P338 |
Num. heavy atoms | 16 |
Num. arom. heavy atoms | 11 |
Fraction Csp3 | 0.0 |
Num. rotatable bonds | 2 |
Num. H-bond acceptors | 2.0 |
Num. H-bond donors | 2.0 |
Molar Refractivity | 66.13 |
TPSA ? Topological Polar Surface Area: Calculated from |
91.56 Ų |
Log Po/w (iLOGP)? iLOGP: in-house physics-based method implemented from |
1.42 |
Log Po/w (XLOGP3)? XLOGP3: Atomistic and knowledge-based method calculated by |
3.62 |
Log Po/w (WLOGP)? WLOGP: Atomistic method implemented from |
3.36 |
Log Po/w (MLOGP)? MLOGP: Topological method implemented from |
2.18 |
Log Po/w (SILICOS-IT)? SILICOS-IT: Hybrid fragmental/topological method calculated by |
3.45 |
Consensus Log Po/w? Consensus Log Po/w: Average of all five predictions |
2.81 |
Log S (ESOL):? ESOL: Topological method implemented from |
-4.07 |
Solubility | 0.0216 mg/ml ; 0.0000851 mol/l |
Class? Solubility class: Log S scale |
Moderately soluble |
Log S (Ali)? Ali: Topological method implemented from |
-5.23 |
Solubility | 0.00149 mg/ml ; 0.00000588 mol/l |
Class? Solubility class: Log S scale |
Moderately soluble |
Log S (SILICOS-IT)? SILICOS-IT: Fragmental method calculated by |
-3.82 |
Solubility | 0.0385 mg/ml ; 0.000152 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) |
Yes |
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 |
-5.28 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 |
0.0 |
Bioavailability Score? Abbott Bioavailability Score: Probability of F > 10% in rat |
0.56 |
PAINS? Pan Assay Interference Structures: implemented from |
0.0 alert |
Brenk? Structural Alert: implemented from |
0.0 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) |
2.6 |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
98% | Stage #1: for 2 h; Heating / reflux Stage #2: With sodium hydrogen sulfate In water |
Example 1; EPO <DP n="24"/>6-(4-Chlorophenyl)-3-{4-[(3i?)-3-hydroxypyrrolidin-l-yl]-3- methoxyphenyl}thieno[3,2-^J[l;,2,3]triazin-4(3J9)-one; a) 3-Amino-5-(4-chIorophenyl)thiophene-2-carboxylic add; Methyl 3-amino-5-(4-chlorophenyl)thiophene-2-carboxylate (2.00 g, 7.47 mmol) was refluxed in a solution of KOH (2.0 g, 36 mmol) in 50 mL of water and 50 mL of MeOH for 2 h. The MeOH was evaporated and the residue was diluted to the double volume with water and washed with ethyl acetate. The aqueous layer was acidified with NaHSO4 (aq) and the precipitate was filtered, washed with water and dried to give 1.85 g (98percent) of the desired compound.1H NMR (DMSO-de) 5 7.62 (m, 2H), 7.48 (m, 2H)3 6.96 (s, IH). |
98% | Stage #1: for 2 h; Heating / reflux Stage #2: With sodium hydrogen sulfate In water |
Example 1; 6-(4-Chlorophenyl)-3-[2-(dimethyIamino)-l-methyl-lET-benzimidazol-6-yl]thieno[3,2- d\\ [l,2,3]triazin-4(3H)-one; a) 3-Amino-5-(4-chIorophenyI)thiophene-2-carboxylic acid; Methyl 3-armno-5-(4-chlorophenyl)thiophene-2-carboxylate (2.00 g, 7.47 mmol) was refluxed in a solution of potassium hydroxide (2.0 g, 36 mmol) in 50 mL of water and 50 mL of methanol for 2 h. Methanol was evaporated and the residue was diluted to the double volume with water and washed with ethyl acetate. The aqueous layer was acidified with NaHSO4 (aq) and the precipitate was filtered, washed with water and dried to give 1.85 g (98percent) of the desired compound. 1H NMR (DMSOd6) δ 7.62 (m, 2H), 7.48 (m, 2H), 6.96 (s, IH). |
98% | Stage #1: for 2 h; Heating / reflux |
Example 1; 6"(4-Chlorophenyl)-3-{4-[2-(3-hydroxypyrrolidin-l-yI)ethoxy]-3- methoxyphenyl}thieno[3,2-rf][l,2,3]triazin-4(3i)-one; a) 3-Amino-5-(4-chIorophenyl)thiophene-2-carboxylic acid; Methyl 3-amino-5-(4-chlorophenyl)thiophene-2-carboxylate (2.00 g, 7.47 rnmol) was refluxed in a solution of potassium hydroxide (2.0 g, 36 mmol) in 50 mL of water and 50 mL of methanol for 2 h. Methanol was evaporated and the residue was diluted to the double volume with water and washed with ethyl acetate. The aqueous layer was acidified with NaHSO4 (aq) and the precipitate was filtered, washed with water and dried to give 1.85 g (98percent) of the desired compound. 1H NMR (DMSO-d6) δ 7.62 (m, 2H), 7.48 (m, 2H), 6.96 (s, IH). |
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