1-amino-1,3-dihydro-2H-indol-2-one

Base Information

• Chemical Name: 1-amino-1,3-dihydro-2H-indol-2-one
• CAS No.: 36149-75-4
• Molecular Formula: C8H8N2O
• Molecular Weight: 148.164
• DSSTox Substance ID: DTXSID50396263
• Nikkaji Number: J89.090A
• Wikidata: Q82196883
• Mol file: 36149-75-4.mol

Synonyms:1-amino-1,3-dihydro-2H-indol-2-one;36149-75-4;1-aminoindolin-2-one;1-amino-3H-indol-2-one;Aminooxindol;amino-oxindole;starbld0025698;SCHEMBL1462133;DTXSID50396263;MHNAXLAGKSOPBH-UHFFFAOYSA-N;1-amino-1,3-dihydro-indol-2-one

Chemical Property of 1-amino-1,3-dihydro-2H-indol-2-one

Chemical Property:

• PSA: 46.33000
• LogP: 1.21470
• XLogP3: 0.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 148.063662883
• Heavy Atom Count: 11
• Complexity: 181

Purity/Quality:

1-AMINO-1,3-DIHYDRO-2H-INDOL-2-ONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C2=CC=CC=C2N(C1=O)N

Technology Process of 1-amino-1,3-dihydro-2H-indol-2-one

There total 6 articles about 1-amino-1,3-dihydro-2H-indol-2-one 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: 70.0%

2'-chloro-benzeneacetic acid (2444-36-2) → 1-amino-1,3-dihydro-2H-indol-2-one (36149-75-4)

Guidance literature:

With copper; hydrazine; In neat (no solvent); at 100 ℃; for 24h; Sealed tube;

DOI:10.1039/c7ra08123e

Reference yield: 54.0%

cinnolin-3(2H)-one (31777-46-5) → 1-amino-1,3-dihydro-2H-indol-2-one (36149-75-4)

Guidance literature:

With sulfuric acid; zinc; In dichloromethane; for 5h; Mechanism; Ambient temperature; also with 15N-labelled compounds;

Reference yield:

1,4-Dihydro-3(2H)-cinnolinone (55116-04-6) → 1-amino-1,3-dihydro-2H-indol-2-one (36149-75-4)

Guidance literature:

With sulfuric acid; In ethanol; for 2h; Yield given; Heating;

upstream raw materials:

(2-hydrazino-phenyl)-acetic acid

cinnolin-3(2H)-one

1,4-Dihydro-3(2H)-cinnolinone

hydrogenchloride

Downstream raw materials:

2-benzyl-3(2H)-cinnolinone

1-(p-methoxybenzylamino)-2-indolinone

1-(p-methylbenzylamino)-2-indolinone

2-(p-methylbenzyl)-3(2H)-cinnolinone