3-Nitroaniline → HCID 11477480, compound

HRID 2247039Notes

Reaction equation

HRID 2247039 reaction equation
O=[C:2]1[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[CH:12][C:11]([N:14]3[CH2:18][C@H:17]([CH2:19][NH:20][C:21](=[O:23])[CH3:22])[O:16][C:15]3=[O:24])=[CH:10][C:9]=2[F:25])[CH2:4][CH2:3]1.[C-:26]#[N:27].[Na+].[N+:29]([C:32]1[CH:33]=[C:34]([CH:36]=[CH:37][CH:38]=1)[NH2:35])([O-:31])=[O:30]>>[N+:29]([C:32]1[CH:33]=[C:34]([NH:35][C:2]2([C:26]#[N:27])[CH2:3][CH2:4][N:5]([C:8]3[CH:13]=[CH:12][C:11]([N:14]4[CH2:18][C@H:17]([CH2:19][NH:20][C:21](=[O:23])[CH3:22])[O:16][C:15]4=[O:24])=[CH:10][C:9]=3[F:25])[CH2:6][CH2:7]2)[CH:36]=[CH:37][CH:38]=1)([O-:31])=[O:30]

Participants

4

Procedure

By using procedure as described in Example 45 and by reacting (S)-N-{3-[4-(4-oxo-piperidin-1-yl)-3-fluorophenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide with sodium cyanide and 3-nitroaniline the compound was obtained in 52% yield.

Workup

  1. customwas obtained in 52% yield

Sources & evidence

ORD record
ord-ce7b1eb7ad93464eaa5d6349f1955eb1
Source dataset
uspto-grants-2010_03
Patent number
US07687627B2

Reaction notes

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