Acetic acid,[[1-[(2S)-2-[[4-[(hydroxyamino)iminomethyl]benzoyl]amino]-1-oxopropyl]-4-piperidinyl]oxy]-(9CI)

Base Information

Chemical Name:Acetic acid,[[1-[(2S)-2-[[4-[(hydroxyamino)iminomethyl]benzoyl]amino]-1-oxopropyl]-4-piperidinyl]oxy]-(9CI)
CAS No.:170096-60-3
Molecular Formula:C₁₈H₂₄N₄O₆
Molecular Weight:392.412
Hs Code.:
Mol file:170096-60-3.mol

Synonyms:Aceticacid, [[1-[2-[[4-[(hydroxyamino)iminomethyl]benzoyl]amino]-1-oxopropyl]-4-piperidinyl]oxy]-,(S)-; Ro 48-3656

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Chemical Property of Acetic acid,[[1-[(2S)-2-[[4-[(hydroxyamino)iminomethyl]benzoyl]amino]-1-oxopropyl]-4-piperidinyl]oxy]-(9CI)

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Technology Process of Acetic acid,[[1-[(2S)-2-[[4-[(hydroxyamino)iminomethyl]benzoyl]amino]-1-oxopropyl]-4-piperidinyl]oxy]-(9CI)

There total 7 articles about Acetic acid,[[1-[(2S)-2-[[4-[(hydroxyamino)iminomethyl]benzoyl]amino]-1-oxopropyl]-4-piperidinyl]oxy]-(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: 86.0%

: 170096-59-0
(1-{(S)-2-[4-(N-Hydroxycarbamimidoyl)-benzoylamino]-propionyl}-piperidin-4-yloxy)-acetic acid tert-butyl ester

: 178740-38-0,170096-60-3
Ro 48-3656

Guidance literature:: With formic acid; at 80 ℃; for 3h;
DOI:10.1021/jm9509298

Reference yield:

: 178601-16-6
{1-[(S)-2-(4-Cyano-benzoylamino)-propionyl]-piperidin-4-yloxy}-acetic acid tert-butyl ester

: 178740-38-0,170096-60-3
Ro 48-3656

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / MeONa, NH₂OH*HCl / methanol / 14 h / 23 °C

2: 86 percent / formic acid / 3 h / 80 °C

With formic acid; hydroxylamine hydrochloride; sodium methylate; In methanol;
DOI:10.1021/jm9509298