N-(2-benzyl-3,4-dihydro-6,7-dimethoxy-2H-1,2-benzothiazine-3-carbonyl)-L-phenylalaninol 1,1-dioxide

Base Information

Chemical Name:N-(2-benzyl-3,4-dihydro-6,7-dimethoxy-2H-1,2-benzothiazine-3-carbonyl)-L-phenylalaninol 1,1-dioxide
CAS No.:376389-39-8
Molecular Formula:C₂₇H₃₀N₂O₆S
Molecular Weight:510.611
Hs Code.:

Synonyms:N-(2-benzyl-3,4-dihydro-6,7-dimethoxy-2H-1,2-benzothiazine-3-carbonyl)-L-phenylalaninol 1,1-dioxide

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Chemical Property of N-(2-benzyl-3,4-dihydro-6,7-dimethoxy-2H-1,2-benzothiazine-3-carbonyl)-L-phenylalaninol 1,1-dioxide

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Technology Process of N-(2-benzyl-3,4-dihydro-6,7-dimethoxy-2H-1,2-benzothiazine-3-carbonyl)-L-phenylalaninol 1,1-dioxide

There total 6 articles about N-(2-benzyl-3,4-dihydro-6,7-dimethoxy-2H-1,2-benzothiazine-3-carbonyl)-L-phenylalaninol 1,1-dioxide 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:

: 3182-95-4
L-Phenylalaninol

: 76685-06-8
3,4-dihydro-6,7-dimethoxy-2-benzyl-2H-1,2-benzothiazine-3-carboxylic acid 1,1-dioxide

: 376389-39-8
N-(2-benzyl-3,4-dihydro-6,7-dimethoxy-2H-1,2-benzothiazine-3-carbonyl)-L-phenylalaninol 1,1-dioxide

Guidance literature:: With 4-methyl-morpholine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; benzotriazol-1-ol; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/jm010178b

Reference yield:

: 14612-07-8
α-Chlor-β-(3,4-dimethoxyphenyl)propionsaeurenitril

: 376389-39-8
N-(2-benzyl-3,4-dihydro-6,7-dimethoxy-2H-1,2-benzothiazine-3-carbonyl)-L-phenylalaninol 1,1-dioxide

Guidance literature:: Multi-step reaction with 5 steps

1: 41 percent / ClSO₃H / CHCl₃ / 5 h / 0 °C

2: 37 percent / NH₃ / dioxane / 2 h / Heating

3: 94 percent / K₂CO₃ / dimethylformamide / 95 - 100 °C

4: 63 percent / 6N aq. NaOH / 0.83 h / Heating

5: HOBt; NMM; BOP / dimethylformamide / 0 - 20 °C

With 4-methyl-morpholine; chlorosulfonic acid; sodium hydroxide; ammonia; potassium carbonate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; benzotriazol-1-ol; In 1,4-dioxane; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jm010178b

Reference yield:

: 76667-04-4
3,4-dihydro-6,7-dimethoxy-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide

: 376389-39-8
N-(2-benzyl-3,4-dihydro-6,7-dimethoxy-2H-1,2-benzothiazine-3-carbonyl)-L-phenylalaninol 1,1-dioxide

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / K₂CO₃ / dimethylformamide / 95 - 100 °C

2: 63 percent / 6N aq. NaOH / 0.83 h / Heating

3: HOBt; NMM; BOP / dimethylformamide / 0 - 20 °C

With 4-methyl-morpholine; sodium hydroxide; potassium carbonate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; benzotriazol-1-ol; In N,N-dimethyl-formamide;
DOI:10.1021/jm010178b