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[ CAS No. 20232-39-7 ] {[proInfo.proName]}

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Chemical Structure| 20232-39-7
Chemical Structure| 20232-39-7
Structure of 20232-39-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 20232-39-7 ]

CAS No. :20232-39-7 MDL No. :MFCD00143492
Formula : C11H14ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :PQXVEYYRJHMTEV-UHFFFAOYSA-N
M.W : 227.69 Pubchem ID :2724664
Synonyms :

Calculated chemistry of [ 20232-39-7 ]

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 66.03
TPSA : 30.82 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.22 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 2.07
Log Po/w (WLOGP) : 2.1
Log Po/w (MLOGP) : 1.31
Log Po/w (SILICOS-IT) : 3.05
Consensus Log Po/w : 1.71

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.72
Solubility : 0.434 mg/ml ; 0.00191 mol/l
Class : Soluble
Log S (Ali) : -2.35
Solubility : 1.03 mg/ml ; 0.0045 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.3
Solubility : 0.114 mg/ml ; 0.000502 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.61

Safety of [ 20232-39-7 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280 UN#:N/A
Hazard Statements:H302+H312+H332 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 20232-39-7 ]

* 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.

  • Upstream synthesis route of [ 20232-39-7 ]
  • Downstream synthetic route of [ 20232-39-7 ]

[ 20232-39-7 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 91342-74-4 ]
  • [ 20232-39-7 ]
  • [ 718635-93-9 ]
YieldReaction ConditionsOperation in experiment
85.6% at 35℃; for 48 h; Large scale 6,7-dimethoxy-3,4-dihydroisoquinoline hydrochloride (118.2 kg) was dissolved in water (3 volumes). 34(Dimethylamino)methyl)-5-methylhexan-2-one (99.1 kg) in n-heptane (1.5 volumes) was added and the mixture stirred vigorously for at least 48 hours at about 35° C. until less than 10percent 6,7-dimethoxy-3,4-dihydroisoquinoline was remaining against a standard solution. The solid was filtered, washed with water then heptane, and then dried under vacuum to provide 3-isobutyl-9,10-dimethoxy-3,4,6,7-tetrahydro-1H-pyrido[2,1-a]isoquinolin-2(11bH)-one (141.1 kg, 85.6percent yield).
79% at 30℃; Large scale The 3-((dimethylamino)methyl)-5-methylhexan-2-one-heptane solution was added to a solution of 6,7-dimethoxy-3,4-dihydroisoquinoline hydrochloride (126.1 kg) in water (315:2 L) and the mixture was stirred at about 30° C. The reaction was judged to be complete when less than 10percent 6,7-dimethoxy-3,4-dihydroisoquinoline was remaining against a standard solution. The mixture was cooled to room temperature and the solids were filtered, washed with water (176.5 L) then n-heptane (277.4 L) both stabilized at a temperature between 15-20° C., and then dried under vacuum to provide 3-isobutyl-9,10-dimethoxy-3,4,6,7-tetrahydro-1H-pyrido[2,1-a]isoquinolin-2(11bH)-one (139 kg, 79percent yield).
73.3% With N-benzyl-N,N,N-triethylammonium chloride In water at 50 - 60℃; for 24 h; Intermediate (3-dimethylaminomethyl-5-methyl-2-hexanone, 30 g, 0.175 mol) and 6,7-dimethoxy-3,4-dihydroisoquinoline hydrochloride (39.8 g, 0.175 mol) was added to 300 ml of water and the catalyst (TEBAC, 4.0 g, 0.018 mol,0.1N), heating reaction. The temperature was controlled at 50-60°C and the reaction time was 24 h. Stop stirring, reduce to room temperature, filter solids, 100mlIt was washed twice with water to give 41.5 g of crude tetrabenazine as an off-white solid in a yield of 81.3percent. Recrystallization from anhydrous ethanol gives tetrabenazineThe refined product was 40.6 g, the total yield was 73.3percent, and the HPLC purity was >99.5percent.
Reference: [1] Patent: US2017/183346, 2017, A1, . Location in patent: Paragraph 0165
[2] Patent: US2017/183346, 2017, A1, . Location in patent: Paragraph 0162; 0164
[3] Patent: CN107698582, 2018, A, . Location in patent: Paragraph 0019
[4] Journal of Labelled Compounds and Radiopharmaceuticals, 2011, vol. 54, # 7, p. 367 - 370
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