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

Triphenylphosphine → HCID 18767693、化合物

HRID 480150
ノート
印刷プレビュー

反応式

HRID 480150 の反応式
[C:1]([CH2:3][CH2:4][NH:5][C:6](=O)[CH2:7][CH2:8][C:9]12[CH2:16][CH2:15][C:12]([C:17]3[NH:25][C:24]4[C:23](=[O:26])[N:22]([CH2:27][CH2:28][CH3:29])[C:21](=[O:30])[N:20]([CH2:31][CH2:32][CH3:33])[C:19]=4[N:18]=3)([CH2:13][CH2:14]1)[CH2:11][CH2:10]2)#[N:2].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[Si]([N:58]=[N+:59]=[N-:60])(C)(C)C.CCOC(/N=N/C(OCC)=O)=O>C1COCC1>[O:30]=[C:21]1[N:20]([CH2:31][CH2:32][CH3:33])[C:19]2[N:18]=[C:17]([C:12]34[CH2:15][CH2:16][C:9]([CH2:8][CH2:7][C:6]5[N:5]([CH2:4][CH2:3][C:1]#[N:2])[N:60]=[N:59][N:58]=5)([CH2:14][CH2:13]3)[CH2:10][CH2:11]4)[NH:25][C:24]=2[C:23](=[O:26])[N:22]1[CH2:27][CH2:28][CH3:29]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 11776TriphenylphosphineHCID 78378AzidotrimethylsilaneHCID 5462977Diethyl azodicarboxylateHCID 18767616HCID 18767616、化合物

生成物 1

HCID 18767693HCID 18767693、化合物収率 3.8%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran
溶媒

実験手順

A solution of N-(2-cyano-ethyl)-3-[4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)-bicyclo[2.2.2]oct-1-yl]-propionamide (500 mg, 1.06 mmol, 1.0 eq), Ph3P (2.0 eq, 2.13 mmol, 560 mg), TMSN3 (2.0 eq, 2.13 mmol, 245 mg), and DEAD (2.0 eq, 2.13 mmol, 371 mg) in THF (10 ml) was stirred at rt for 24 h. The reaction vessel was re-charged with the reagent cocktail (2.0 eq, 2.13 mmol) and stirring was continued for an additional 24 h. The reaction was quenched by the addition of a 5% aqueous solution of (NH4)2Ce(NO3)6 and extracted with EtOAc. The combined organic extracts were washed with brine, dried over MgSO4, filtered and evaporated in vacuo to afford a viscous orange oil. A portion of the material was purified by preparative LC to afford 20 mg of pure material. MS: 494 (MH+).

後処理

  1. additionThe reaction vessel was re-charged with the reagent cocktail (2.0 eq, 2.13 mmol)
  2. customThe reaction was quenched by the addition of a 5% aqueous solution of (NH4)2Ce(NO3)6
  3. extractionextracted with EtOAc
  4. washThe combined organic extracts were washed with brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customevaporated in vacuo
  8. customto afford a viscous orange oil
  9. customA portion of the material was purified by preparative LC

出典と根拠

ORDレコード
ord-39fd8894da9545d5a2f514953ce67010
出典データセット
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06649600B1

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