Hydrochloric Acid → ethyl 1-(2-ethoxy-2-iminoethyl)-5-methyl-1H-pyrrole-2-carboxylate hydrochloride

HRID 77364

반응식

HRID 77364 반응식
[C:1]([CH2:3][N:4]1[C:8]([CH3:9])=[CH:7][CH:6]=[C:5]1[C:10]([O:12][CH2:13][CH3:14])=[O:11])#[N:2].[ClH:15].[CH2:16]([O:18]CC)[CH3:17].C(O)C>>[ClH:15].[CH2:16]([O:18][C:1](=[NH:2])[CH2:3][N:4]1[C:8]([CH3:9])=[CH:7][CH:6]=[C:5]1[C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH3:17]

참가 물질

5

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온도
0 °C

실험 절차

A high pressure reaction vessel charged with ethyl 1-(cyanomethyl)-5-methyl-1H-pyrrole-2-carboxylate (848 mg, 4.41 mmol) cooled to 0° C. was treated with a 2M solution of hydrochloric acid in diethyl ether (30 mL, 60 mmol) and absolute ethanol (406 mg, 8.82 mmol). The mixture was stirred at 0° C. for 10 min and then was warmed to room temperature where it stirred over the weekend. At this time, the mixture was diluted with hexanes. The resulting precipitate was collected by filtration to afford ethyl 1-(2-ethoxy-2-iminoethyl)-5-methyl-1H-pyrrole-2-carboxylate hydrochloride (1.16 g, 95.7%) as a white solid. LC-MS calcd. for C12H19N2O3 [(M+H)+] 239, obsd. 239.0.

후처리

  1. customA high pressure reaction vessel
  2. temperaturewas warmed to room temperature where it
  3. stirringstirred over the weekend
  4. filtrationThe resulting precipitate was collected by filtration

출처 및 근거

ORD 기록
ord-74d36ae72802488f9990d44583f7963c
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08841299B2

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