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

Nitrogen → 17-[2-(3-Fluoro-phenyl)-7-methoxy-8-methyl-quinazolin-4-yloxy]-13-methyl-2,14-dioxo-3,13,15-triaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid ethyl ester

HRID 1443509
ノート
印刷プレビュー

反応式

HRID 1443509 の反応式
C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[CH2:20]([O:22][C:23]([C:25]12[CH2:42][CH:41]1[CH:40]=[CH:39][CH2:38][CH2:37][CH2:36][CH2:35][N:34]([CH3:43])[C:33](=[O:44])[N:32]1[CH:28]([CH2:29][CH:30]([OH:45])[CH2:31]1)[C:27](=[O:46])[NH:26]2)=[O:24])[CH3:21].[F:47][C:48]1[CH:49]=[C:50]([C:54]2[N:63]=[C:62](O)[C:61]3[C:56](=[C:57]([CH3:67])[C:58]([O:65][CH3:66])=[CH:59][CH:60]=3)[N:55]=2)[CH:51]=[CH:52][CH:53]=1.N#N.CC(OC(/N=N/C(OC(C)C)=O)=O)C>C1COCC1.CN(C=O)C>[CH2:20]([O:22][C:23]([C:25]12[CH2:42][CH:41]1[CH:40]=[CH:39][CH2:38][CH2:37][CH2:36][CH2:35][N:34]([CH3:43])[C:33](=[O:44])[N:32]1[CH:28]([CH2:29][CH:30]([O:45][C:62]3[C:61]4[C:56](=[C:57]([CH3:67])[C:58]([O:65][CH3:66])=[CH:59][CH:60]=4)[N:55]=[C:54]([C:50]4[CH:51]=[CH:52][CH:53]=[C:48]([F:47])[CH:49]=4)[N:63]=3)[CH2:31]1)[C:27](=[O:46])[NH:26]2)=[O:24])[CH3:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 947NitrogenHCID 11776TriphenylphosphineHCID 5363146Diisopropyl azodicarboxylateHCID 6841037217-Hydroxy-13-methyl-2,14-dioxo-3,13,15-triaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid ethyl esterHCID 1784877302-(3-fluorophenyl)-7-methoxy-8-methyl-1H-quinazolin-4-one

生成物 1

HCID 68687309
17-[2-(3-Fluoro-phenyl)-7-methoxy-8-methyl-quinazolin-4-yloxy]-13-methyl-2,14-dioxo-3,13,15-triaza-tricyclo[13.3.0.0*4,6*]octadec-7-ene-4-carboxylic acid ethyl ester
収率 75%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

PPh3 (415 mg, 1.58 mmol) was added to a stirred solution of the alcohol 51 (300 mg, 0.79 mmol) and the quinazolinol 127 (247 mg, 0.87 mmol) in dry THF (35 mL) and dry DMF 7 mL. The reaction was placed under an inert atmosphere (N2) at room temperature. DIAD (311 μL, 1.58 mmol) was added. The reaction mixture was stirred for 18 h. A precipitation was formed in the flask and more white solid precipitated after addition of 40 mL diethyl ether. The precipitation was filtered off and washed with diethyl ether and dried under vacuum which gave the pure title compound (381 mg, 75%). LRMS (M+H) 646.

後処理

  1. customA precipitation
  2. customwas formed in the flask and more white solid
  3. customprecipitated
  4. additionafter addition of 40 mL diethyl ether
  5. customThe precipitation
  6. filtrationwas filtered off
  7. washwashed with diethyl ether
  8. customdried under vacuum which

出典と根拠

ORDレコード
ord-051228f4746c4f98947d57ae389962f3
出典データセット
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07659245B2

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