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

tert-Butanol → HCID 136181547、化合物

HRID 848717
ノート
印刷プレビュー

反応式

HRID 848717 の反応式
[P:1]([O:5][C@@H:6]1[C@@H:10]([CH2:11][OH:12])[O:9][C@@H:8]([N:13]2[C:23]3[N:22]=[C:20]([NH2:21])[NH:19][C:17](=[O:18])[C:16]=3[N:15]=[CH:14]2)[C@@H:7]1[OH:24])(O)([OH:3])=[O:2].C(O)(C)(C)C.C1([N:36]=C=NC2CCCCC2)CCCCC1>O.N.C(N)=O>[P:1]([O:5][C@@H:6]1[C@@H:10]([CH2:11][OH:12])[O:9][C@@H:8]([N:13]2[C:23]3[N:22]=[C:20]([NH2:21])[NH:19][C:17](=[O:18])[C:16]=3[N:15]=[CH:14]2)[C@@H:7]1[OH:24])([NH2:36])(=[O:2])[OH:3]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6386tert-ButanolHCID 10868DicyclohexylcarbodiimideHCID 1353987273'-Gmp

生成物 1

HCID 136181547HCID 136181547、化合物収率 50%

試薬・触媒・溶媒 2

HCID 713Formamide溶媒HCID 12896473Azane;hydrate溶媒

反応条件

温度
80 °C

実験手順

Three millimoles of guanosine-3'-monophosphate were dissolved in a mixture of 7.5 ml of 2 N ammonia water and 5 ml of formamide, the solution was combined with 20 ml of tertiary butanol that contained 15 millimoles of dicyclohexyl carbodiimide, and the resulting mixture was heated at 80° C. for a period of 9 to 10 hours with care taken to prevent evaporation of the solvent. After the reaction, the mixture was left to stand overnight at room temperature, the precipitate was filtered off, the filtrate was concentrated under vacuum to remove the tertiary butanol, and the residue was extracted with ether. The aqueous layer was recovered, concentrated under vacuum, and the residue was treated with acetone to give a crystal of guanosine-3'-monophosphoramidate in a yield of about 50%. The crystal was heated under vacuum at 100° C. for a period of 3 to 4 hours until it was dehydrated thoroughly.

後処理

  1. customevaporation of the solvent
  2. customAfter the reaction
  3. waitthe mixture was left
  4. filtrationthe precipitate was filtered off
  5. concentrationthe filtrate was concentrated under vacuum
  6. customto remove the tertiary butanol
  7. extractionthe residue was extracted with ether
  8. customThe aqueous layer was recovered
  9. concentrationconcentrated under vacuum
  10. additionthe residue was treated with acetone

出典と根拠

ORDレコード
ord-5b8ab559fab44be59b1a9b64a6a36ec8
出典データセット
uspto-grants-1981_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04297347

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート