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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Acetic Acid → HCID 178419920、化合物

HRID 1382576
ノート
印刷プレビュー

反応式

HRID 1382576 の反応式
COC([N:5]1[CH2:10][CH2:9][CH:8]([C:11]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[NH:13][N:12]=2)[CH2:7][CH2:6]1)=N.C(O)(=O)C>O>[NH:5]1[CH2:6][CH2:7][CH:8]([C:11]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[NH:13][N:12]=2)[CH2:9][CH2:10]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 176Acetic AcidHCID 1784968134-(1H-indazol-3-yl)piperidine-1-carboximidic acid methyl ester

生成物 1

HCID 178419920HCID 178419920、化合物収率 46.4%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A solution of 4.7 g of 4-(1H-indazol-3-yl)piperidine-1-carboximidic acid methyl ester and 80% of acetic acid was heated under reflux for 48 hrs. The reaction mixture was cooled and poured into water. The aqueous phase was extracted with ether and then made basic by the slow addition of a 50% aqueous sodium hydroxide soluton. A solid separated from the solution. The solid was collected and dried. Recrystallization from ethanol yielded 1.7 g (46%) of product. Concentration of the mother liquors from this and another experiment gave additional product, mp 213°-215° C.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureunder reflux for 48 hrs
  2. temperatureThe reaction mixture was cooled
  3. extractionThe aqueous phase was extracted with ether
  4. additionmade basic by the slow addition of a 50% aqueous sodium hydroxide soluton
  5. customA solid separated from the solution
  6. customThe solid was collected
  7. customdried
  8. customRecrystallization from ethanol

出典と根拠

ORDレコード
ord-c6778f95086d4cb6b4012bd3ceba41e4
出典データセット
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04806649

反応ノート

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