Diisopropylethylamine → Trifluoroacetic acid

HRID 1920551ノート

反応式

HRID 1920551 の反応式
[F:1][C:2]([F:7])([F:6])[C:3]([O-:5])=[O:4].[C:8]([CH2:11][N+:12]12[CH2:19][CH2:18][CH:15]([CH2:16][CH2:17]1)[C@@H:14]([O:20][C:21](=[O:36])[C:22]([OH:35])([C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)[CH2:13]2)([OH:10])=O.CCN(C(C)C)C(C)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.Cl.[CH2:71]([C:73]1[CH:74]=[C:75]2[C:79](=[CH:80][C:81]=1[CH2:82][CH3:83])[CH2:78][CH:77]([NH2:84])[CH2:76]2)[CH3:72]>CN(C=O)C>[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].[F:1][C:2]([F:7])([F:6])[C:3]([O-:5])=[O:4].[CH2:82]([C:81]1[CH:80]=[C:79]2[C:75](=[CH:74][C:73]=1[CH2:71][CH3:72])[CH2:76][CH:77]([NH:84][C:8]([CH2:11][N+:12]13[CH2:17][CH2:16][CH:15]([CH2:18][CH2:19]1)[CH:14]([O:20][C:21](=[O:36])[C:22]([OH:35])([C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1)[CH2:13]3)=[O:10])[CH2:78]2)[CH3:83]

参加物

7

実験手順

To a stirred suspension of (R)-1-carboxymethyl-3-(2-hydroxy-2,2-diphenyl-acetoxy)-1-azonia-bicyclo[2.2.2]octane trifluoroacetate [Ex. 62] (0.052 g, 0.102 mmol) in dry DMF (5 ml) is added DIPEA (0.070 ml, 0.408 mmol), HATU (0.097 g, 0.255 mmol) and 5,6-Diethyl-indan-2-ylamine hydrochloride (0.058 g, 0.255 mmol). The mixture is left to stir at room temperature overnight. The solvent is removed in vacuo and purification by mass directed preparative HPLC eluting with acetonitrile:water:trifluoroacetic acid yields the titled compound.

後処理

  1. waitThe mixture is left
  2. customThe solvent is removed in vacuo and purification by mass
  3. washeluting with acetonitrile

出典と根拠

ORDレコード
ord-c1c0347ae59249a297c783f5877baa0c
出典データセット
uspto-grants-2012_05
特許番号
US08168654B2

反応ノート

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