4-Hydrazinylpyridine hydrochloride → N-[2-(4-Benzyloxyphenyl)ethylidene]-N'-pyridin-4-ylhydrazine hydrochloride monohydrate

HRID 612458

반응식

HRID 612458 반응식
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH:15]=[CH:16]OC)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[ClH:19].[NH:20]([C:22]1[CH:27]=[CH:26][N:25]=[CH:24][CH:23]=1)[NH2:21]>C(O)C.C1(C)C=CC(S(O)(=O)=O)=CC=1>[OH2:8].[ClH:19].[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH:16]=[N:21][NH:20][C:22]2[CH:27]=[CH:26][N:25]=[CH:24][CH:23]=2)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

5

반응물 2

HCID 223202584-Hydrazinylpyridine hydrochlorideHCID 538954501-(4-Benzyloxyphenyl)-2-methoxyethylene

생성물 1

HCID 70106552N-[2-(4-Benzyloxyphenyl)ethylidene]-N'-pyridin-4-ylhydrazine hydrochloride monohydrate수율 120.4%

시약·촉매·용매 2

HCID 6101p-Toluenesulfonic acid촉매HCID 702Ethanol용매

실험 절차

A mixture of 1-benzyloxy-4-(2-methoxyvinyl)benzene (16.9 g), 4-hydrazinopyridine hydrochloride (11.3 g) and p-toluenesulfonic acid (0.68 g) in ethanol (200 ml) was heated under reflux for 5 hrs, with stirring. The reaction mixture was cooled, filtered, and the filtrate was concentrated in vacuo. The residue crystallized to give 15.75 g (63%) of product, mp 203-205° C.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 5 hrs
  3. temperatureThe reaction mixture was cooled
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated in vacuo
  6. customThe residue crystallized

출처 및 근거

ORD 기록
ord-664c4c0414f4464d83b98a997d99930d
출처 데이터셋
uspto-grants-1999_12
특허 번호
US06004977

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