5-Benzoyl-6-(methylsulfanyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid

Base Information

Chemical Name:5-Benzoyl-6-(methylsulfanyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid
CAS No.:89542-09-6
Molecular Formula:C16H15NO3S
Molecular Weight:301.366
Hs Code.:
ChEMBL ID:CHEMBL277428
DSSTox Substance ID:DTXSID50546766

Synonyms:89542-09-6;CHEMBL277428;SCHEMBL10810361;DTXSID50546766;WWBBGICOHFLYSR-UHFFFAOYSA-N;5-Benzoyl-6-(methylsulfanyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid;5-benzoyl-6-methylthio-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid

Suppliers and Price of 5-Benzoyl-6-(methylsulfanyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-Benzoyl-6-(methylsulfanyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:301.07726451
Heavy Atom Count:21
Complexity:422

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CSC1=C(N2CCC(C2=C1)C(=O)O)C(=O)C3=CC=CC=C3

Technology Process of 5-Benzoyl-6-(methylsulfanyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid

There total 8 articles about 5-Benzoyl-6-(methylsulfanyl)-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid 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: 77.0%

: 89542-05-2
5-Benzoyl-6-methylsulfanyl-2,3-dihydro-1H-pyrrolizine-1-carbonitrile

: 89542-09-6
5-benzoyl-6-methylthio-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid

Guidance literature:: With sodium hydroxide; In ethanol; water; for 8h; Heating;
DOI:10.1021/jm00126a010

Reference yield:

: 76786-72-6
1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carbonitrile

: 89542-09-6
5-benzoyl-6-methylthio-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid

Guidance literature:: Multi-step reaction with 7 steps

1: 1) N-chlorosuccinimide (NCS) / 1) dichloromethane, -10 deg C, 10 min, 2) dichloromethane, -55 deg C to r.t.

2: toluene / 0.33 h / Heating

3: 97 percent / sodium periodate / methanol; H₂O / 3 h / Ambient temperature

4: 97 percent / trifluoroacetic acid / CH₂Cl₂ / 1.83 h / Ambient temperature

5: iodine, triphenylphosphine, sodium iodide / acetonitrile / 0.08 h

6: 84 percent / xylene / 20 h / Heating

7: 77 percent / sodium hydroxide / ethanol; H₂O / 8 h / Heating

With sodium hydroxide; sodium periodate; N-chloro-succinimide; iodine; triphenylphosphine; trifluoroacetic acid; sodium iodide; In methanol; ethanol; dichloromethane; water; toluene; acetonitrile; xylene;
DOI:10.1021/jm00126a010

Reference yield:

: 89541-93-5
6-(methylthio)-1,2-dihydro-3H-pyrrolo<1,2-a>pyrrole-1-carbonitrile

: 89542-09-6
5-benzoyl-6-methylthio-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / xylene / 20 h / Heating

2: 77 percent / sodium hydroxide / ethanol; H₂O / 8 h / Heating

With sodium hydroxide; In ethanol; water; xylene;
DOI:10.1021/jm00126a010