Isopropyl isocyanate → 3-[[2-(4-Morpholinyl)ethyl]methylamino]-1,2-benzisoxazol-6-yl 1-methylethylcarbamate

HRID 582863ノート

反応式

HRID 582863 の反応式
[N:1]1([CH2:7][CH2:8][N:9]([CH3:20])[C:10]2[C:14]3[CH:15]=[CH:16][C:17]([OH:19])=[CH:18][C:13]=3[O:12][N:11]=2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[CH3:21][CH:22]([N:24]=[C:25]=[O:26])[CH3:23].CO.C(Cl)Cl>CCOC(C)=O.[Cu]Cl>[CH3:21][CH:22]([NH:24][C:25](=[O:26])[O:19][C:17]1[CH:16]=[CH:15][C:14]2[C:10]([N:9]([CH2:8][CH2:7][N:1]3[CH2:6][CH2:5][O:4][CH2:3][CH2:2]3)[CH3:20])=[N:11][O:12][C:13]=2[CH:18]=1)[CH3:23]

参加物

6

実験手順

To a stirred solution of 3-[[2-(4-morpholinyl)ethyl]-methylamino]-1,2-benzisoxazol-6-ol (2.2 g) and copper(I)chloride (0.1 g) in EtOAc (50 ml) was added 1-methylethylisocyanate (0.8 g). After 24 hours TLC (silica gel, 10% MeOH/DCM) showed no starting material. The reaction was filtered through neutral alumina eluting with EtOAc (3 l) and the filtrate was concentrated in vacuo. The white solid was flash chromatographed on silica gel eluting with 1% MeOH/DCM to yield 1.2 g of the product, m.p. 99-100° C.

後処理

  1. filtrationThe reaction was filtered through neutral alumina eluting with EtOAc (3 l)
  2. concentrationthe filtrate was concentrated in vacuo
  3. customchromatographed on silica gel eluting with 1% MeOH/DCM

出典と根拠

ORDレコード
ord-f89235da09b14b26bb7a8677a8d6a3d2
出典データセット
uspto-grants-1999_07
特許番号
US05925766

反応ノート

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