(6R)-7t-benzoylamino-3-methyl-8-oxo-7c-succinimido-(6rH)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

Base Information

• Chemical Name: (6R)-7t-benzoylamino-3-methyl-8-oxo-7c-succinimido-(6rH)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester
• CAS No.: 73786-46-6
• Molecular Formula: C₃₂H₂₇N₃O₇
• Molecular Weight: 565.582
• Mol file: 73786-46-6.mol

Synonyms:

Chemical Property of (6R)-7t-benzoylamino-3-methyl-8-oxo-7c-succinimido-(6rH)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (6R)-7t-benzoylamino-3-methyl-8-oxo-7c-succinimido-(6rH)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

There total 6 articles about (6R)-7t-benzoylamino-3-methyl-8-oxo-7c-succinimido-(6rH)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester 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:

N-chloro-succinimide (128-09-6) + (6R)-7c-benzoylamino-3-methyl-8-oxo-(6rH)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester (68314-20-5) → (6R)-7t-benzoylamino-3-methyl-8-oxo-7c-succinimido-(6rH)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester (73786-46-6)

Guidance literature:

With bromine; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; at 25 ℃;

DOI:10.1016/S0040-4039(01)86579-5

Reference yield:

epi-Secopenicillin (67977-61-1,68107-98-2) → (6R)-7t-benzoylamino-3-methyl-8-oxo-7c-succinimido-(6rH)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester (73786-46-6)

Guidance literature:

Multi-step reaction with 4 steps

1: NBS / acetone; H₂O / 15 °C

2: BF₃-Et₂O / ethyl acetate; CH₂Cl₂ / 25 °C

3: DBU / CH₂Cl₂ / -20 °C

4: Br₂, DBU / tetrahydrofuran / 25 °C

With N-Bromosuccinimide; boron trifluoride diethyl etherate; bromine; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; dichloromethane; water; ethyl acetate; acetone;

DOI:10.1016/S0040-4039(01)86579-5

Reference yield:

(2R,3Ξ)-3,4-dihydroxy-3-methyl-2-((1R)-7-oxo-3-phenyl-(1rH,5cH)-4-oxa-2,6-diaza-bicyclo[3.2.0]hept-2-en-6-yl)-butyric acid benzhydryl ester (68313-65-5,68539-32-2,68539-33-3) → (6R)-7t-benzoylamino-3-methyl-8-oxo-7c-succinimido-(6rH)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester (73786-46-6)

Guidance literature:

Multi-step reaction with 3 steps

1: BF₃-Et₂O / CH₂Cl₂ / 25 °C

2: SOCl₂, Py / CH₂Cl₂ / 0.5 h / 25 °C

3: Br₂, DBU / tetrahydrofuran / 25 °C

With pyridine; thionyl chloride; boron trifluoride diethyl etherate; bromine; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; dichloromethane;

DOI:10.1016/S0040-4039(01)86579-5

upstream raw materials:

N-chloro-succinimide

(6R)-7c-benzoylamino-3-methyl-8-oxo-(6rH)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester

epi-Secopenicillin

(2R,3Ξ)-3,4-dihydroxy-3-methyl-2-((1R)-7-oxo-3-phenyl-(1rH,5cH)-4-oxa-2,6-diaza-bicyclo[3.2.0]hept-2-en-6-yl)-butyric acid benzhydryl ester