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[ CAS No. 61700-61-6 ] {[proInfo.proName]}

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Chemical Structure| 61700-61-6
Chemical Structure| 61700-61-6
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Product Details of [ 61700-61-6 ]

CAS No. :61700-61-6 MDL No. :MFCD06804570
Formula : C8H6N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :MAVGBUDLHOOROM-UHFFFAOYSA-N
M.W : 162.15 Pubchem ID :4248454
Synonyms :

Calculated chemistry of [ 61700-61-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 43.05
TPSA : 65.98 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.43 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.55
Log Po/w (XLOGP3) : 1.21
Log Po/w (WLOGP) : 1.26
Log Po/w (MLOGP) : 0.72
Log Po/w (SILICOS-IT) : 1.38
Consensus Log Po/w : 1.02

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.1
Solubility : 1.3 mg/ml ; 0.00801 mol/l
Class : Soluble
Log S (Ali) : -2.19
Solubility : 1.04 mg/ml ; 0.00642 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.27
Solubility : 0.863 mg/ml ; 0.00532 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.14

Safety of [ 61700-61-6 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 61700-61-6 ]

* 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.

  • Downstream synthetic route of [ 61700-61-6 ]

[ 61700-61-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 61700-61-6 ]
  • [ 1086391-06-1 ]
  • 2
  • [ 98121-41-6 ]
  • [ 61700-61-6 ]
  • [ 1619884-66-0 ]
YieldReaction ConditionsOperation in experiment
93% With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; at 20℃; A solution of the respective 1H-indazole-5-carboxylic acid or 1-alkyl-1H-indazole-5-carboxylic acid (1 or 7, 10, 1.0 mmol), 3,4-dichaloaniline or <strong>[98121-41-6]5,6-dichloropyridin-3-amine</strong> (-5 or 6,1.1-1.2 mmol), N-ethyl-N-(3-dimethylaminopropyl)carbodiimidehydrochloride (EDC-HCl, 1.0-1.2 mmol) in methanol (5.0 mL) wasstirred over night at room temperature. The reaction was thenpoured into water (10 mL), stirred for 30 min at room temperature,filtered, washed with water (3 x 10 mL), and then dried at 70 C.The crude product was purified by column chromatography onsilica gel (mobile phase: dichloromethane/MeOH 9/1 v/v) following by recrystallization from petroleum ether/dichloromethane. 4.1.2.1. N-(5,6-dichloropyridin-3-yl)-1H-indazole-5-carboxamide(14). Off-white-greyish solid (125 mg, 93%); mp > 290 C (dec.). 1HNMR (500 MHz, DMSO-d6) delta 7.67 (d, J 8.82 Hz, 1H, Ph), 8.05 (d,J 8.51 Hz, 1H, Ph), 8.21 (s, 1H, Ind.-Het.), 8.34 (s, 1H, Pyr.), 8.44 (s,1H, Ph), 8.74 (s, 1H, Pyr), 12.8 (s, 1H, CONH), 13.55 (s, 1H, NH). 13CNMR (125 MHz, DMSO-d6) delta 110.1, 111.1, 120.5, 123.0, 123.2, 123.9,126.3, 126.7, 127.1, 135.3, 136.1, 141.4, 163.1. ESI-MS (m/z): calcd. forC13H8Cl2N4O: 306.008; found 305.121 [M H]e, 307.301 [M H].
  • 3
  • [ 61700-61-6 ]
  • [ 885521-46-0 ]
YieldReaction ConditionsOperation in experiment
84% With iodine; potassium hydroxide; In N,N-dimethyl-formamide; at 25℃; for 3h; Into a 25-mL round-bottom flask was placed 1 H-indazole-5-carboxylic acid (200 mg, 1.23 mmol), Nu,Nu-dimethylformamide (3 ml_), potassium hydroxide (138 mg, 2.46 mmol) and iodine (470 mg, 1.85 mmol). The solution was stirred for 3 h at 25C. The reaction was quenched by the addition of 10 mL of Na2S203. The pH value of the solution was adjusted to 6 with hydrogen chloride solution (10 %). The solids were collected by filtration. This resulted in 300 mg (84%) of 3-iodo-1 H-indazole-5-carboxylic acid as a white solid
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