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LORCASERIN

LORCASERIN Structure
CAS No.
616202-92-7
Chemical Name:
LORCASERIN
Synonyms
Apd356;Ar-10a;CS-1994;Apd-356;Apd 356;LORCASERIN;LORCASERIN API;Unii-637E494o0z;Lorcaserin powder;Lotcaserin Freebase
CBNumber:
CB61011744
Molecular Formula:
C11H14ClN
Molecular Weight:
195.69
MOL File:
616202-92-7.mol
MSDS File:
SDS
Modify Date:
2023/9/7 19:13:26

LORCASERIN Properties

Boiling point 288 ºC
Density 1.075
Flash point 128 ºC
storage temp. -20°C Freezer
solubility Chloroform (Slightly), Methanol (Slightly)
form Light Beige to Beige Semi-Solid
pka 9.99±0.40(Predicted)
Stability Hygroscopic
InChI InChI=1S/C11H14ClN/c1-8-7-13-5-4-9-2-3-10(12)6-11(8)9/h2-3,6,8,13H,4-5,7H2,1H3/t8-/m0/s1
InChIKey XTTZERNUQAFMOF-QMMMGPOBSA-N
SMILES N1CCC2=CC=C(Cl)C=C2[C@@H](C)C1

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS09
Signal word  Warning
Hazard statements  H410-H302
Precautionary statements  P264-P270-P301+P312-P330-P501-P273-P391-P501

LORCASERIN Chemical Properties,Uses,Production

Chemical Properties

Yellow Oil

Uses

Lorcaserin was used to treat Opioid Use Disorder (OUD).

Definition

ChEBI: A benzazepine that is 2,3,4,5-tetrahydro-3-benzazepine substituted at position 1 by a methyl group and a t position 6 by a chloro group.

Mechanism of action

Lorcaserin acts at 5-HT2C receptors in the central nervous system (CNS), particularly the hypothalamus, to reduce appetite.

Side effects

  • constipation
  • dry mouth
  • excessive tiredness
  • pain in the back or muscles
  • headache
  • dizziness
  • difficulty falling asleep or staying asleep
  • anxiety

Synthesis

The synthesis of LORCASERIN is as follows:
Liquid precursor 53 11-HCl (0.5mmol) was placed into a test tube equipped with a magnetic stir bar. Anhydrous 44 AlCl3 (1.75 equiv according to starting material) was added and efficiently mixed to obtain a paste. The mixture was slowly heated (10°C/min) to 150°C and stirred overnight. A saturated solution of 54 NaCl was added and the mixture was cooled. The pH was adjusted to 9.5-10 using 1M NaOH and then extracted with EtOAc. The combined organic phases were washed with brine, dried over Na2SO4 and the solvent was evaporated under reduced pressure. The obtained crude mixture was analyzed using 1H NMR spectroscopy (estimated yield by 1H NMR was 62%).
synthesis of LORCASERIN.png

LORCASERIN Preparation Products And Raw materials

Raw materials

Preparation Products

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Apd 356 Apd356 Apd-356 Ar-10a Unii-637E494o0z LORCASERIN (R)-8-Chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine (1R)-8-Chloro-2,3,4,5-tetrahydro-1-Methyl-1H-3-benzazepine Lotcaserin Freebase APD 356;APD356;APD-356;AR-10A;APD-356;APD 356;APD356 CS-1994 LORCASERIN USP/EP/BP cas856681-05-5 (1R)-8-Chloro-2,3,4,5-tetrahydro-1-methyl-1H-3-benzazepine Lorcaserin(free base) Lorcaserin powder Lorcaserin D4 MaleateQ: What is Lorcaserin D4 Maleate Q: What is the CAS Number of Lorcaserin D4 Maleate Q: What is the storage condition of Lorcaserin D4 Maleate Q: What are the applications of Lorcaserin D4 Maleate LorcaserinQ: What is Lorcaserin Q: What is the CAS Number of Lorcaserin Q: What is the storage condition of Lorcaserin LORCASERIN API 616202-92-7 16202-92-7 Amines Aromatics Chiral Reagents Heterocycles Intermediates & Fine Chemicals Pharmaceuticals 616202-92-7