4-amino-2-(2-(azetidin-1-yl)-2-oxoethyl)-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxabor-6-yl)benzenesulfonamide

Base Information

Chemical Name:4-amino-2-(2-(azetidin-1-yl)-2-oxoethyl)-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxabor-6-yl)benzenesulfonamide
CAS No.:1308255-15-3
Molecular Formula:C₁₈H₂₀BN₃O₅S
Molecular Weight:401.251
Hs Code.:

Synonyms:4-amino-2-(2-(azetidin-1-yl)-2-oxoethyl)-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxabor-6-yl)benzenesulfonamide

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Chemical Property of 4-amino-2-(2-(azetidin-1-yl)-2-oxoethyl)-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxabor-6-yl)benzenesulfonamide

Chemical Property:

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Technology Process of 4-amino-2-(2-(azetidin-1-yl)-2-oxoethyl)-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxabor-6-yl)benzenesulfonamide

There total 8 articles about 4-amino-2-(2-(azetidin-1-yl)-2-oxoethyl)-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxabor-6-yl)benzenesulfonamide 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:

: 1308254-89-8
2-(5-amino-2-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)phenyl)acetic acid

: 78797-58-7,78797-59-8,78797-62-3,36520-39-5,65546-09-0
azetidine hydrochloride

: 1308255-15-3
4-amino-2-(2-(azetidin-1-yl)-2-oxoethyl)-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxabor-6-yl)benzenesulfonamide

Guidance literature:: With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; triethylamine; In N,N-dimethyl-formamide; for 3h;

Reference yield:

: 52913-11-8
(3-amino-phenyl)-acetic acid methyl ester

: 1308255-15-3
4-amino-2-(2-(azetidin-1-yl)-2-oxoethyl)-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxabor-6-yl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: 2,6-dimethylpyridine / dichloromethane / 2 h / 0 - 20 °C

2: chlorosulfonic acid / 2 h / 0 - 20 °C / Neat (no solvent)

3: 4-methyl-morpholine / acetonitrile / 0 - 20 °C

4: sodium hydroxide; water / methanol / 16 h / 20 °C

5: triethylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 3 h

With 4-methyl-morpholine; 2,6-dimethylpyridine; chlorosulfonic acid; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; water; triethylamine; sodium hydroxide; In methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 3958-57-4
1-bromomethyl-3-nitrobenzene

: 1308255-15-3
4-amino-2-(2-(azetidin-1-yl)-2-oxoethyl)-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxabor-6-yl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 8 steps

1: N,N-dimethyl-formamide / 5 h / 50 °C

2: hydrogenchloride / methanol / 20 °C

3: hydrogenchloride; iron / water; methanol / 20 °C

4: 2,6-dimethylpyridine / dichloromethane / 2 h / 0 - 20 °C

5: chlorosulfonic acid / 2 h / 0 - 20 °C / Neat (no solvent)

6: 4-methyl-morpholine / acetonitrile / 0 - 20 °C

7: sodium hydroxide; water / methanol / 16 h / 20 °C

8: triethylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 3 h

With 4-methyl-morpholine; 2,6-dimethylpyridine; hydrogenchloride; chlorosulfonic acid; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; water; iron; triethylamine; sodium hydroxide; In methanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;