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Draft:Spiclomazine

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Spiclomazine
Clinical data
Other namesClospirazine, APY-606, Disepron.
Identifiers
  • 8-[3-(2-chlorophenothiazin-10-yl)propyl]-1-thia-4,8-diazaspiro[4.5]decan-3-one
CAS Number
PubChem CID
ChemSpider
UNII
ChEBI
ChEMBL
Chemical and physical data
FormulaC22H24ClN3OS2
Molar mass446.02 g·mol−1
3D model (JSmol)
  • C1CN(CCC12NC(=O)CS2)CCCN3C4=CC=CC=C4SC5=C3C=C(C=C5)Cl
  • InChI=InChI=1S/C22H24ClN3OS2/c23-16-6-7-20-18(14-16)26(17-4-1-2-5-19(17)29-20)11-3-10-25-12-8-22(9-13-25)24-21(27)15-28-22/h1-2,4-7,14H,3,8-13,15H2,(H,24,27)
  • Key:CFOYBMUYCBSDAL-UHFFFAOYSA-N
Spiclomazine
Clinical data
Other namesClospirazine, APY-606, Disepron.
Identifiers
CAS Number
PubChem CID
ChemSpider
Chemical and physical data
FormulaC22H24ClN3OS2
Molar mass446.02 g·mol−1
3D model (JSmol)
  • C1CN(CCC12NC(=O)CS2)CCCN3C4=CC=CC=C4SC5=C3C=C(C=C5)Cl

Neuroleptic Tranquilliser (used in treatment of schizophrenia).

Pharmacol:[1][2] Antineoplastic:[3]

Synthesis

[edit]

A chemical synthesis is proposed:[4][5][6]

Spiclomazine synthesis
Spiclomazine synthesis

The reaction between the hydrochloride of 4-piperidone [41661-47-6] HCl H2O [40064-34-4] (1), ammonium carbonate [506-87-6] (2) and thioglycolic acid [68-11-1] (3) gives 1-thia-4,8-diazaspiro[4.5]decan-3-one, PC10419642 (4). The alkylation of the last with 2-chloro-10-(3-chloropropyl)phenothiazine [2765-59-5] (5) completed the synthesis of Spiclomazine (6)

References

[edit]
  1. ^ Nakanishi M, Okada T, Tsumagari T (July 1970). "[Studies on psychotropic drugs. V. Pharmacological effects of 8-(3-(2-chloro-10-phenothiazinyl)propyl)-1-thia-4,8-diazaspiro(4,5) decan-3-one hydrochloride (APY-606)]". Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan (in Japanese). 90 (7): 800–7. doi:10.1248/yakushi1947.90.7_800. PMID 5465390.
  2. ^ Nakanishi M, Okada T, Kato Y (July 1970). "[Studies on psychotropic drugs. VI. Metabolic fate of APY-606. (1). Excretion and metabolism in rats]". Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan (in Japanese). 90 (7): 808–12. doi:10.1248/yakushi1947.90.7_808. PMID 5465391.
  3. ^ Zhao W, Li D, Liu Z, Zheng X, Wang J, Wang E (2013). "Spiclomazine induces apoptosis associated with the suppression of cell viability, migration and invasion in pancreatic carcinoma cells". PLOS ONE. 8 (6): e66362. doi:10.1371/journal.pone.0066362. PMC 3688794. PMID 23840452.
  4. ^ Michio Nakanishi, Katsuo Arimura, Tatsumi Tsumagari Masa Shiroki, US3574204 (1971 to Yoshitomi Pharmaceutical).
  5. ^ Katsuo Arimura, Michio Nakanishi, Tadao Okada, US3661902 (1972 to Yoshitomi Pharmaceutical).
  6. ^ Michio Nakanishi, et al. US3651052 (1972 to Welfide Corp).