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Triethylamine → 3-Methoxycarbonylethylcarbonyloxy-1-phenylindole hydrochloride

HRID 1194397
ノート
印刷プレビュー

反応式

HRID 1194397 の反応式
[ClH:1].C(N(CC(O)CNC([C:13]1[N:14]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:15]2[C:20]([C:21]=1[OH:22])=[CH:19][CH:18]=[CH:17][CH:16]=2)=O)CC)C.C(N(CC)CC)C.[Cl-].[CH3:38][O:39][C:40](=[O:46])[CH2:41][CH2:42][C:43](O)=[O:44]>C(Cl)Cl>[ClH:1].[CH3:38][O:39][C:40]([CH2:41][CH2:42][C:43]([O:22][C:21]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[N:14]([C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)[CH:13]=1)=[O:44])=[O:46]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 547241132-[3-(N,N-diethylamino)-2-hydroxypropylaminocarbonyl]-3-hydroxy-1-phenylindole hydrochlorideHCID 86605420Succinic acid methylester chloride

生成物 1

HCID 867428213-Methoxycarbonylethylcarbonyloxy-1-phenylindole hydrochloride

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

2.1 g of 2-[3-(N,N-diethylamino)-2-hydroxypropylaminocarbonyl]-3-hydroxy-1-phenylindole hydrochloride (0.005 mole) are mixed in 25 ml of methylene chloride with 0.7 ml triethylamine (0.005 mole) and 0.6 ml of succinic acid methylester chloride and the reaction mixture agitated for 1 h at room temperature. The solution is then washed with a saturated solution of sodium chloride, dried over sodium sulfate, filtered and evaporated. The residue is purified by low pressure chromatography using methylene chloride as the elution agent, as described in Example 3. 2-[3-N,N-diethylamino)-2-hydroxypropylaminocarbonyl]-3-methoxycarbonylethylcarbonyloxy-1-phenylindole hydrochloride is obtained as an oily product.

後処理

  1. washThe solution is then washed with a saturated solution of sodium chloride
  2. dry with materialdried over sodium sulfate
  3. filtrationfiltered
  4. customevaporated
  5. customThe residue is purified by low pressure chromatography

出典と根拠

ORDレコード
ord-d81c6409718e4dbbaa0a27e706b50e8a
出典データセット
uspto-grants-1989_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04814345

反応ノート

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