N-(2-Trityl-1,2,3,4-tetrahydro-isoquinolin-7-ylmethyl)-methanesulfonamide

Base Information

Chemical Name:N-(2-Trityl-1,2,3,4-tetrahydro-isoquinolin-7-ylmethyl)-methanesulfonamide
CAS No.:200137-84-4
Molecular Formula:C₃₀H₃₀N₂O₂S
Molecular Weight:482.646
Hs Code.:

Synonyms:N-(2-Trityl-1,2,3,4-tetrahydro-isoquinolin-7-ylmethyl)-methanesulfonamide

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Chemical Property of N-(2-Trityl-1,2,3,4-tetrahydro-isoquinolin-7-ylmethyl)-methanesulfonamide

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Technology Process of N-(2-Trityl-1,2,3,4-tetrahydro-isoquinolin-7-ylmethyl)-methanesulfonamide

There total 5 articles about N-(2-Trityl-1,2,3,4-tetrahydro-isoquinolin-7-ylmethyl)-methanesulfonamide 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: 88.4%

: 124-63-0
methanesulfonyl chloride

: 200137-83-3
C-(2-Trityl-1,2,3,4-tetrahydro-isoquinolin-7-yl)-methylamine

: 200137-84-4
N-(2-Trityl-1,2,3,4-tetrahydro-isoquinolin-7-ylmethyl)-methanesulfonamide

Guidance literature:: With triethylamine; In dichloromethane; for 16h; Ambient temperature;
DOI:10.1021/jm960235e

Reference yield:

: 99365-69-2
7-nitro-1,2,3,4-tetrahydroisoquinoline hydrochloride

: 200137-84-4
N-(2-Trityl-1,2,3,4-tetrahydro-isoquinolin-7-ylmethyl)-methanesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: 92.2 percent / H₂, conc. HCl / PtO₂ / aq. ethanol / 4 h / 2585.7 Torr

2: 1.) aq. NaNO₂, conc. HCl, 2.) aq. NaOH, Ni₂SO₄*6H₂O / 1.) from 0 deg C to 5 deg C, 15 min, 2.) benzene, a) from 5 deg C to RT, 2 h, b) from RT to 50 deg C, 1 h

3: 86.7 percent / Et₃N, DMAP / CH₂Cl₂ / 14 h

4: 76.9 percent / BH₃*THF / tetrahydrofuran / 18 h / Heating

5: 88.4 percent / Et₃N / CH₂Cl₂ / 16 h / Ambient temperature

With hydrogenchloride; dmap; sodium hydroxide; borane-THF; O₄S^(2-)*2Ni⁽¹⁺⁾; hydrogen; triethylamine; sodium nitrite; platinum(IV) oxide; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/jm960235e

Reference yield:

: 72299-68-4
1,2,3,4-Tetrahydro-isoquinolin-7-ylamine

: 200137-84-4
N-(2-Trityl-1,2,3,4-tetrahydro-isoquinolin-7-ylmethyl)-methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) aq. NaNO₂, conc. HCl, 2.) aq. NaOH, Ni₂SO₄*6H₂O / 1.) from 0 deg C to 5 deg C, 15 min, 2.) benzene, a) from 5 deg C to RT, 2 h, b) from RT to 50 deg C, 1 h

2: 86.7 percent / Et₃N, DMAP / CH₂Cl₂ / 14 h

3: 76.9 percent / BH₃*THF / tetrahydrofuran / 18 h / Heating

4: 88.4 percent / Et₃N / CH₂Cl₂ / 16 h / Ambient temperature

With hydrogenchloride; dmap; sodium hydroxide; borane-THF; O₄S^(2-)*2Ni⁽¹⁺⁾; triethylamine; sodium nitrite; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm960235e