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3-amino-1-benzylindolin-2-one hydrochloride

Base Information Edit
  • Chemical Name:3-amino-1-benzylindolin-2-one hydrochloride
  • CAS No.:1324055-93-7
  • Molecular Formula:C15H14N2O*ClH
  • Molecular Weight:274.75
  • Hs Code.:
  • Mol file:1324055-93-7.mol
3-amino-1-benzylindolin-2-one hydrochloride

Synonyms:3-amino-1-benzylindolin-2-one hydrochloride

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Chemical Property of 3-amino-1-benzylindolin-2-one hydrochloride Edit
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Technology Process of 3-amino-1-benzylindolin-2-one hydrochloride

There total 5 articles about 3-amino-1-benzylindolin-2-one hydrochloride 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:
Guidance literature:
Multi-step reaction with 2 steps
1: palladium 10% on activated carbon; hydrogen / methanol / 10 h / 20 °C / 760.05 Torr
2: hydrogenchloride / methanol
With hydrogenchloride; palladium 10% on activated carbon; hydrogen; In methanol;
DOI:10.1021/ol200724q
Guidance literature:
Multi-step reaction with 2 steps
1.1: hydroxylamine hydrochloride / water / 0.5 h / Reflux
1.2: 0.5 h / Reflux
2.1: palladium 10% on activated carbon; hydrogen / methanol / 10 h / 20 °C / 760.05 Torr
With palladium 10% on activated carbon; hydroxylamine hydrochloride; hydrogen; In methanol; water;
DOI:10.1016/j.tet.2018.11.016
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydride / N,N-dimethyl-formamide / 20 °C
2.1: hydroxylamine hydrochloride / water / 0.5 h / Reflux
2.2: 0.5 h / Reflux
3.1: palladium 10% on activated carbon; hydrogen / methanol / 10 h / 20 °C / 760.05 Torr
With palladium 10% on activated carbon; hydroxylamine hydrochloride; hydrogen; sodium hydride; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2018.11.016
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