Technology Process of [13C9]-2,5-dichloro-N-(2-(((R)-3-methyl-1-((3αS,4S,6S,7αR)-3α,5,5-trimethylhexahydro-4,6-methanobenzo[d][1,3,2]dioxaborol-2-yl)butyl)amino)-2-oxoethyl)benzamide
There total 3 articles about [13C9]-2,5-dichloro-N-(2-(((R)-3-methyl-1-((3αS,4S,6S,7αR)-3α,5,5-trimethylhexahydro-4,6-methanobenzo[d][1,3,2]dioxaborol-2-yl)butyl)amino)-2-oxoethyl)benzamide 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:
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1310383-72-2,179324-87-9
(aR,3aS,4S,6S,7aR)-hexahydro-3a,8,8-trimethyl-α-(2-methylpropyl)-4,6-methano-1,3,2-benzodioxaborole-2-methanamine 2,2,2-trifluoroacetate
- Guidance literature:
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(aR,3aS,4S,6S,7aR)-hexahydro-3a,8,8-trimethyl-α-(2-methylpropyl)-4,6-methano-1,3,2-benzodioxaborole-2-methanamine 2,2,2-trifluoroacetate; [13C9]-[(2,5-dichlorobenzoyl)amino]acetic acid;
With
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate;
In
N,N-dimethyl-formamide;
at 20 ℃;
for 0.25h;
Inert atmosphere;
With
N-ethyl-N,N-diisopropylamine;
In
N,N-dimethyl-formamide;
at 0 ℃;
for 1h;
Inert atmosphere;
DOI:10.1002/jlcr.3079
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: sodium hydroxide / tetrahydrofuran; water / 20 °C
2.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 0.25 h / 20 °C / Inert atmosphere
2.2: 1 h / 0 °C / Inert atmosphere
With
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; sodium hydroxide;
In
tetrahydrofuran; water; N,N-dimethyl-formamide;
1.1: |Schotten-Baumann Reaction;
DOI:10.1002/jlcr.3079
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: aluminum (III) chloride / 5 h / 47 - 100 °C / Inert atmosphere
2.1: sodium hydroxide; sodium hypochlorite; water / 1,4-dioxane / 72 h / 0 - 25 °C
3.1: thionyl chloride / 2 h / 50 °C / Inert atmosphere
4.1: sodium hydroxide / tetrahydrofuran; water / 20 °C
5.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 0.25 h / 20 °C / Inert atmosphere
5.2: 1 h / 0 °C / Inert atmosphere
With
aluminum (III) chloride; sodium hypochlorite; thionyl chloride; water; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; sodium hydroxide;
In
tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide;
1.1: |Friedel-Crafts Alkylation / 2.1: |Haloform Reaction / 4.1: |Schotten-Baumann Reaction;
DOI:10.1002/jlcr.3079
