6-amino-7-nitro-N-<4-(morpholinosulfonyl)benzyl>-1,2,3,4-tetrahydroquinoline

Base Information

Chemical Name:6-amino-7-nitro-N-<4-(morpholinosulfonyl)benzyl>-1,2,3,4-tetrahydroquinoline
CAS No.:138814-41-2
Molecular Formula:C₂₀H₂₄N₄O₅S
Molecular Weight:432.5
Hs Code.:

Synonyms:6-amino-7-nitro-N-<4-(morpholinosulfonyl)benzyl>-1,2,3,4-tetrahydroquinoline

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Chemical Property of 6-amino-7-nitro-N-<4-(morpholinosulfonyl)benzyl>-1,2,3,4-tetrahydroquinoline

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Technology Process of 6-amino-7-nitro-N-<4-(morpholinosulfonyl)benzyl>-1,2,3,4-tetrahydroquinoline

There total 6 articles about 6-amino-7-nitro-N-<4-(morpholinosulfonyl)benzyl>-1,2,3,4-tetrahydroquinoline 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: 89.0%

: 138814-52-5
6-(acetylamino)-7-nitro-N-<4-(morpholinosulfonyl)benzyl>-1,2,3,4-tetrahydroquinoline

: 138814-41-2
6-amino-7-nitro-N-<4-(morpholinosulfonyl)benzyl>-1,2,3,4-tetrahydroquinoline

Guidance literature:: With hydrogenchloride; at 60 ℃; for 5.5h;
DOI:10.1021/jm00083a007

Reference yield:

: 580-15-4
6-aminoquinoline

: 138814-41-2
6-amino-7-nitro-N-<4-(morpholinosulfonyl)benzyl>-1,2,3,4-tetrahydroquinoline

Guidance literature:: Multi-step reaction with 5 steps

1: 77 percent / CH₂Cl₂ / 0.17 h / 25 °C

2: 85 percent / H₂ / PtO₂ / acetic acid / 1.5 h / 1551.4 Torr

3: 98percent H₂SO₄, 70percent HNO₃ / -10 °C

4: 84 percent / diisopropylethylamine / dimethylformamide / 5 h / 70 °C

5: 89 percent / 3 N aq. HCl / 5.5 h / 60 °C

With hydrogenchloride; sulfuric acid; hydrogen; nitric acid; N-ethyl-N,N-diisopropylamine; platinum(IV) oxide; In dichloromethane; acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jm00083a007

Reference yield:

: 22433-76-7
N-(Quinolin-6-yl)acetamide

: 138814-41-2
6-amino-7-nitro-N-<4-(morpholinosulfonyl)benzyl>-1,2,3,4-tetrahydroquinoline

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / H₂ / PtO₂ / acetic acid / 1.5 h / 1551.4 Torr

2: 98percent H₂SO₄, 70percent HNO₃ / -10 °C

3: 84 percent / diisopropylethylamine / dimethylformamide / 5 h / 70 °C

4: 89 percent / 3 N aq. HCl / 5.5 h / 60 °C

With hydrogenchloride; sulfuric acid; hydrogen; nitric acid; N-ethyl-N,N-diisopropylamine; platinum(IV) oxide; In acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jm00083a007