1H-Pyrrolo[1,2-c]imidazole-1,3(2H)-dione,tetrahydro-6-hydroxy-,(6R)-(9CI)

Base Information

Chemical Name:1H-Pyrrolo[1,2-c]imidazole-1,3(2H)-dione,tetrahydro-6-hydroxy-,(6R)-(9CI)
CAS No.:198084-54-7
Molecular Formula:C₆H₈N₂O₃
Molecular Weight:156.141
Hs Code.:
Mol file:198084-54-7.mol

Synonyms:1H-Pyrrolo[1,2-c]imidazole-1,3(2H)-dione,tetrahydro-6-hydroxy-,(6R)-(9CI)

Suppliers and Price of 1H-Pyrrolo[1,2-c]imidazole-1,3(2H)-dione,tetrahydro-6-hydroxy-,(6R)-(9CI)

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of 1H-Pyrrolo[1,2-c]imidazole-1,3(2H)-dione,tetrahydro-6-hydroxy-,(6R)-(9CI)

Chemical Property:

PKA:12.71±0.40(Predicted)
PSA：73.13000
Density:1.59±0.1 g/cm3(Predicted)
LogP:-1.11480

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1H-Pyrrolo[1,2-c]imidazole-1,3(2H)-dione,tetrahydro-6-hydroxy-,(6R)-(9CI)

There total 1 articles about 1H-Pyrrolo[1,2-c]imidazole-1,3(2H)-dione,tetrahydro-6-hydroxy-,(6R)-(9CI) 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:

: 590-28-3
potassium cyanate

: 51-35-4,30724-02-8
4R-4-hydroxyproline

: 198084-54-7
7-hydroxy-1,3-diazabicyclo[3.3.0]octane-2,4-dione

Guidance literature:: With hydrogenchloride; triethylamine; Yield given. Multistep reaction; 1) H₂O, 80 deg C, 2 h, 2) H₂O, reflux, 7 h;
DOI:10.1002/ardp.19973300808

Reference yield: 90.0%

: 198084-54-7
7-hydroxy-1,3-diazabicyclo[3.3.0]octane-2,4-dione

: 74-88-4
methyl iodide

: 198084-55-8
7-hydroxy-3-methyl-1,3-diazabicyclo[3.3.0]octane-2,4-dione

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 65 ℃; for 3h;
DOI:10.1002/ardp.19973300808

Reference yield:

: 198084-54-7
7-hydroxy-1,3-diazabicyclo[3.3.0]octane-2,4-dione

: 198084-60-5
p-nitrobenzyl (1R,5S,6S)-6-((1R)-1-hydroxyethyl)-2-((5R,7S)-3-methyl-1,3-diazabicyclo[3.3.0]octane-2,4-dion-7-ylthio)-1-methylcarbapen-2-em-3-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / K₂CO₃ / dimethylformamide / 3 h / 65 °C

2: 84 percent / Et₃N / CH₂Cl₂ / 1 h / 0 °C

3: 79.1 percent / dimethylformamide; toluene / 3 h / 65 °C

4: 39.1 percent / 4 N NaOH / methanol / 0.17 h / 0 °C

5: 39 percent / iPr₂NEt / acetonitrile / 2 h / 0 °C

With sodium hydroxide; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1002/ardp.19973300808