Dipropargylamine → 2,4-Bis-benzyloxy-5-isopropenyl-N,N-di-prop-2-ynyl-benzamide

HRID 241829ノート

反応式

HRID 241829 の反応式
[CH2:1]([O:8][C:9]1[CH:17]=[C:16]([O:18][CH2:19]C2C=CC=CC=2)[C:15]([C:26]([CH3:28])=[CH2:27])=[CH:14][C:10]=1[C:11]([OH:13])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.C(N=C=NCCCN(C)C)C.ON1[C:46]2[CH:47]=[CH:48][CH:49]=[CH:50][C:45]=2N=N1.[CH2:51]([NH:54][CH2:55][C:56]#[CH:57])[C:52]#[CH:53]>ClCCl>[CH2:1]([O:8][C:9]1[CH:17]=[C:16]([O:18][CH2:19][C:45]2[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=2)[C:15]([C:26]([CH3:28])=[CH2:27])=[CH:14][C:10]=1[C:11]([N:54]([CH2:55][C:56]#[CH:57])[CH2:51][C:52]#[CH:53])=[O:13])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

6

実験手順

A stirred solution of 2,4-bis-benzyloxy-5-isopropenyl-benzoic acid (Example 1 Step 6) (1 equivalent) in dichloromethane (10 ml) was treated successively with N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.2 equivalents), 1-hydroxybenzotriazole (1.2 equivalents) and dipropargylamine (1.5 equivalents) and the mixture was stirred at room temperature overnight. The mixture was washed successively with 2M hydrochloric acid and 2M sodium hydroxide, the organic layer was separated and the solvent removed in vacuo to afford the product which was either obtained pure or was purified by column chromatography on silica (eluting with mixtures of ethyl acetate in petroleum ether or methanol in ethyl acetate as appropriate). MS: [M+H]+ 450

後処理

  1. washThe mixture was washed successively with 2M hydrochloric acid and 2M sodium hydroxide
  2. customthe organic layer was separated
  3. customthe solvent removed in vacuo
  4. customto afford the product which
  5. customwas purified by column chromatography on silica (eluting with mixtures of ethyl acetate in petroleum ether or methanol in ethyl acetate as appropriate)

出典と根拠

ORDレコード
ord-67924166b19a4afabc46ba53151dc276
出典データセット
uspto-grants-2014_02
特許番号
US08653084B2

反応ノート

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