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[ CAS No. 26116-12-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Chemical Structure| 26116-12-1
Chemical Structure| 26116-12-1
Structure of 26116-12-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 26116-12-1 ]

CAS No. :26116-12-1 MDL No. :MFCD00003178
Formula : C7H16N2 Boiling Point : -
Linear Structure Formula :H2NCH2(C4NH7)C2H5 InChI Key :UNRBEYYLYRXYCG-UHFFFAOYSA-N
M.W : 128.22 Pubchem ID :117295
Synonyms :
Chemical Name :2-(Aminomethyl)-1-ethylpyrrolidine

Calculated chemistry of [ 26116-12-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.17
TPSA : 29.26 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.96
Log Po/w (XLOGP3) : 0.24
Log Po/w (WLOGP) : 0.05
Log Po/w (MLOGP) : 0.57
Log Po/w (SILICOS-IT) : 0.57
Consensus Log Po/w : 0.68

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -0.65
Solubility : 28.4 mg/ml ; 0.222 mol/l
Class : Very soluble
Log S (Ali) : -0.41
Solubility : 49.3 mg/ml ; 0.385 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.89
Solubility : 16.4 mg/ml ; 0.128 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.51

Safety of [ 26116-12-1 ]

Signal Word:Danger Class:3,8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:2733
Hazard Statements:H225-H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 26116-12-1 ]

* 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.

  • Downstream synthetic route of [ 26116-12-1 ]

[ 26116-12-1 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 26116-12-1 ]
  • [ 19641-29-3 ]
  • 6-Chloro-2-(1-ethyl-pyrrolidin-2-ylmethyl)-2,3-dihydro-isoindol-1-one [ No CAS ]
  • 2
  • [ 26116-12-1 ]
  • [ 72411-89-3 ]
  • [ 72412-44-3 ]
  • 3
  • [ 498-63-5 ]
  • [ 26116-12-1 ]
  • 4
  • [ 26116-12-1 ]
  • [ 71675-87-1 ]
  • [ 541-41-3 ]
  • [ 71675-85-9 ]
YieldReaction ConditionsOperation in experiment
61% With triethylamine; In water; acetone; N-(1-ethyl 2-pyrrolidylmethyl) 2-methoxy 4-amino 5-ethylsulphonyl benzamide 81 g of <strong>[71675-87-1]2-methoxy 4-amino 5-ethylsulphonyl benzoic acid</strong> and 297 cm3 of acetone are placed in a flask fitted with an agitator, a thermometer and a dropping funnel, followed by 33 g of triethylamine. The solution is cooled to 0° C., then 30 g of ethyl chloroformate is added drop by drop between 0° and 5° C. When the mixture has been agitated 51 g of 1-ethyl 2-amino methyl pyrrolidine is added drop by drop between 5° and 10° C. The mixture is agitated at 10° C. then at ambient temperature. The triethylamine hydrochloride which precipitates is drained, then the acetone is distilled. The residue is dissolved in 600 cm3 of water in the presence of caustic soda solution. The base crystallises after seeding and is drained, washed with water and dried. When the crystals have been purified by passing them through hydrochloride and re-crystallising them in acetone, 66 g of N-[1-ethyl 2-pyrrolidylmethyl] 2-methoxy 4-amino 5-ethylsulphonyl benzamide is obtained (yield 61percent-M.P.=126° to 127° C.).
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