ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
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
  1. ホーム
  2. /反応

Hydrochloric Acid → HCID 20525070、化合物

HRID 1702794
ノート
印刷プレビュー

反応式

HRID 1702794 の反応式
[ClH:1].C(OC([NH:9][CH2:10][CH2:11][CH2:12][NH:13][C:14]([N:16]1[CH:23]=[C:22]([F:24])[C:20](=[O:21])[NH:19][C:17]1=[O:18])=[O:15])=O)(C)(C)C>C(O)C>[ClH:1].[NH2:9][CH2:10][CH2:11][CH2:12][NH:13][C:14]([N:16]1[CH:23]=[C:22]([F:24])[C:20](=[O:21])[NH:19][C:17]1=[O:18])=[O:15]
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 313Hydrochloric AcidHCID 20525037HCID 20525037、化合物

生成物 1

HCID 20525070HCID 20525070、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Hydrogen chloride gas was introduced to the solution of 1-[N-[3-(t-butoxycarbonylamino)propyl]carbamoyl]-5-fluorouracil (5.1 g.) which was prepared in Example 20 in ethanol (30 ml.) until precipitates were appeared for 1 hour with stirring under cooling with ice. The reaction mixture was further stirred for 1 hour at ambient temperature, and diethyl ether (100 ml.) was added therein. The resultant crystalline precipitates were collected by filtration and were dried over phosphoric anhydride to give 1-[N-(3-aminopropyl)carbamoyl]-5-fluorouracil hydrochloride (1.5 g.).

後処理

  1. customuntil precipitates
  2. temperatureunder cooling with ice
  3. stirringThe reaction mixture was further stirred for 1 hour at ambient temperature
  4. additiondiethyl ether (100 ml.) was added
  5. customThe resultant crystalline precipitates
  6. filtrationwere collected by filtration
  7. dry with materialwere dried over phosphoric anhydride

出典と根拠

ORDレコード
ord-7d3ced70ccde4ad9858aa0392fd45052
出典データセット
uspto-grants-1982_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04349552

反応ノート

読み込み中…

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