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

Sodium Carbonate → HCID 24894616、化合物

HRID 254747
ノート
印刷プレビュー

反応式

HRID 254747 の反応式
ClC1N=C(NC(C2C=CC3C(=CC=CC=3)C=2)C)N=C(N)N=1.NC(CC1C=CC(B2OC(C)(C)C(C)(C)O2)=CN=1)C(O)=O.C(=O)([O-])[O-].[Na+].[Na+].[NH2:49][CH:50]([CH2:54][C:55]1[CH:60]=[CH:59][C:58]([C:61]2[N:66]=[C:65]([NH2:67])[N:64]=[C:63]([NH:68][CH:69]([C:71]3[CH:80]=[CH:79][C:78]4[C:73](=[CH:74][CH:75]=[CH:76][CH:77]=4)[CH:72]=3)[CH3:70])[N:62]=2)=[CH:57][N:56]=1)[C:51]([OH:53])=[O:52]>Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.O.C(#N)C>[NH2:49][C@@H:50]([CH2:54][C:55]1[CH:60]=[CH:59][C:58]([C:61]2[N:66]=[C:65]([NH2:67])[N:64]=[C:63]([NH:68][C@@H:69]([C:71]3[CH:80]=[CH:79][C:78]4[C:73](=[CH:74][CH:75]=[CH:76][CH:77]=4)[CH:72]=3)[CH3:70])[N:62]=2)=[CH:57][N:56]=1)[C:51]([OH:53])=[O:52]
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

8

反応物 4

HCID 10340Sodium CarbonateHCID 66653554HCID 66653554、化合物HCID 74338134HCID 74338134、化合物HCID 131728137HCID 131728137、化合物

生成物 1

HCID 24894616HCID 24894616、化合物

試薬・触媒・溶媒 3

HCID 178418476HCID 178418476、化合物
触媒
HCID 962Water溶媒
HCID 6342Acetonitrile溶媒

反応条件

温度
150 °C

実験手順

A microwave vial was charged with 6-chloro-N-[1-naphthalen-2yl-ethyl]-[1,3,5]triazine-2,4-diamine (30 mg, 0.1 mmol), 2-boc protected-amino-3-{5-[4,4,5,5,-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridin2-yl-]-propionic acid (50 mg, 0.15 mmol) 1 ml of acetonitrile, and 0.7 ml of water. Aqueous sodium carbonate (0.3 ml; 1N) was added to the solution, followed by 5 mol percent dichlorobis(triphenylphosphine)-palladium(II). The reaction vessel was sealed and heated to 150° C. for 5 minutes by microwave. After cooling, the reaction mixture was evaporated to dryness. The residue was dissolved in 2.5 ml of methanol, and was then purified by Prep-LC to give 7 mg of boc protected 2-amino-3-{5-[4-amino-6-(1-naphthalen-2-yl-ethylamino)-[1,3,5]triazin-2-yl]-pyridin-2-yl}proionic acid.

後処理

  1. customThe reaction vessel was sealed
  2. temperatureAfter cooling
  3. customthe reaction mixture was evaporated to dryness
  4. dissolutionThe residue was dissolved in 2.5 ml of methanol
  5. customwas then purified by Prep-LC
  6. customto give 7 mg of boc

出典と根拠

ORDレコード
ord-553bf1199b944833b1d220b77e997056
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07875622B2

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