4-(N-Methylaminomethyl)-9-isopropyl-2,3,4,9-tetrahydrothiopyrano(2,3-b)indole hydrochloride

Base Information

Chemical Name:4-(N-Methylaminomethyl)-9-isopropyl-2,3,4,9-tetrahydrothiopyrano(2,3-b)indole hydrochloride
CAS No.:73426-10-5
Molecular Formula:C₁₇H₂₄N₂S*ClH
Molecular Weight:324.918
Hs Code.:
DSSTox Substance ID:DTXSID90994181

Synonyms:Thiopyrano(2,3-b)indole-4-methylamine, 2,3,4,9-tetrahydro-9-isobutyl-N-methyl-, HCl;4-(N-Methylaminomethyl)-9-isopropyl-2,3,4,9-tetrahydrothiopyrano(2,3-b)indole hydrochloride;9-Isobutyl-N-methyl-2,3,4,9-tetrahydrothiopyrano(2,3-b)indole-4-methylamine hydrochloride;Thiopyrano(2,3-b)indole-4-methanamine, 2,3,4,9-tetrahydro-N-methyl-9-(2-methylpropyl)-, HCl;73426-10-5;Thiopyrano(2,3-a)indole, 2,3,4,9-tetrahydro-9-isobutyl-4-((methylamino)methyl)-, monohydrochloride;C17H24N2S.ClH;DTXSID90994181;C17-H24-N2-S.Cl-H;LS-153295;1-[9-(3-Methylbutyl)-2,3,4,9-tetrahydrothiopyrano[2,3-b]indol-4-yl]methanamine--hydrogen chloride (1/1)

Suppliers and Price of 4-(N-Methylaminomethyl)-9-isopropyl-2,3,4,9-tetrahydrothiopyrano(2,3-b)indole hydrochloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-(N-Methylaminomethyl)-9-isopropyl-2,3,4,9-tetrahydrothiopyrano(2,3-b)indole hydrochloride

Chemical Property:

Vapor Pressure:6.04E-08mmHg at 25°C
Boiling Point:440.1°C at 760 mmHg
Flash Point:220°C
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:324.1426977
Heavy Atom Count:21
Complexity:320

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)CCN1C2=CC=CC=C2C3=C1SCCC3CN.Cl

Technology Process of 4-(N-Methylaminomethyl)-9-isopropyl-2,3,4,9-tetrahydrothiopyrano(2,3-b)indole hydrochloride

There total 3 articles about 4-(N-Methylaminomethyl)-9-isopropyl-2,3,4,9-tetrahydrothiopyrano(2,3-b)indole hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 73425-49-7
4-aminomethyl-2,3,4,9-tetrahydrothiopyrano<2,3-b>indole

: 73426-10-5
4-(N-methylaminomethyl)-9-isobutyl-2,3,4,9-tetrahydrothiopyrano<2,3-b>indole hydrichoride

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / Et₃N / tetrahydrofuran / 1 h / Ambient temperature

2: 1) 50 percent NaH / 1.) oil, DMF, RT, 1 h; 2.) DMF, oil

3: 1) CF₃COOH; 2) HCl / CH₂Cl₂ / 2 h

With hydrogenchloride; sodium hydride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1248/cpb.32.877

Reference yield:

: 73425-25-9
4-(N-tert-butoxycarbonyl-N-methylaminomethyl)-2,3,4,9-tetrahydrothiopyrano<2,3-b>indole

: 73426-10-5
4-(N-methylaminomethyl)-9-isobutyl-2,3,4,9-tetrahydrothiopyrano<2,3-b>indole hydrichoride

Guidance literature:: Multi-step reaction with 2 steps

1: 1) 50 percent NaH / 1.) oil, DMF, RT, 1 h; 2.) DMF, oil

2: 1) CF₃COOH; 2) HCl / CH₂Cl₂ / 2 h

With hydrogenchloride; sodium hydride; trifluoroacetic acid; In dichloromethane;
DOI:10.1248/cpb.32.877