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Potassium Carbonate → HCID 70980960、化合物

HRID 1468694
ノート
印刷プレビュー

反応式

HRID 1468694 の反応式
[C:1]([O:7][CH2:8][C@H:9]([C:15]1[C:26]([CH3:27])=[CH:25][C:18]2[N:19]=[C:20]([CH:22]3[CH2:24][CH2:23]3)[S:21][C:17]=2[C:16]=1Br)[O:10][C:11]([CH3:14])([CH3:13])[CH3:12])(=[O:6])[C:2]([CH3:5])([CH3:4])[CH3:3].[O:29]1[C:40]2[C:41]3[C:36]([C:37](B(O)O)=[CH:38][CH:39]=2)=[N:35][CH:34]=[CH:33][C:32]=3[CH2:31][CH2:30]1.C([O-])([O-])=O.[K+].[K+]>CC(N(C)C)=O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[C:1]([O:7][CH2:8][C@@H:9]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])[C:15]1[C:26]([CH3:27])=[CH:25][C:18]2[N:19]=[C:20]([CH:22]3[CH2:24][CH2:23]3)[S:21][C:17]=2[C:16]=1[C:37]1[C:36]2[C:41]3=[C:32]([CH2:31][CH2:30][O:29][C:40]3=[CH:39][CH:38]=1)[CH:33]=[CH:34][N:35]=2)(=[O:6])[C:2]([CH3:5])([CH3:4])[CH3:3]
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 3

HCID 11430Potassium CarbonateHCID 59578523HCID 59578523、化合物HCID 70981621HCID 70981621、化合物

生成物 1

HCID 70980960HCID 70980960、化合物

試薬・触媒・溶媒 2

HCID 178418397HCID 178418397、化合物触媒HCID 31374
Dimethylacetamide
溶媒

実験手順

To a solution of (S)-2-(7-bromo-2-cyclopropyl-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyethyl pivalate (18) (23 mg, 0.047 mmol) in DMA (2 ml), was added 2,3-dihydropyrano[4,3,2-de]quinolin-7-ylboronic acid (25 mg, 0.099 mmol), 2N K2CO3 solution (0.11 ml, 0.22 mmol) and Pd(PPh3)4 (6 mg, 0.005 mmol). The reaction mixture was reacted at 85° C. for 2 hs. The reaction was cooled down, washed by saturated NaHCO3 solution, extracted by EtOAc. The organic phase was combined, dry over MgSO4, filtered, concentrated and purified by silica gel column, eluting by 0-50% EtOAc in hexanes. Two isomers were separated and went through the chemistry sequence as above. LCMS-ESI+: calc'd for C33H38N2O4S: 559.2 (M+H+). Found: 559.1 (M+H+).

後処理

  1. customThe reaction mixture was reacted at 85° C. for 2 hs
  2. temperatureThe reaction was cooled down
  3. washwashed by saturated NaHCO3 solution
  4. extractionextracted by EtOAc
  5. dry with materialdry over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. custompurified by silica gel column
  9. washeluting by 0-50% EtOAc in hexanes
  10. customTwo isomers were separated

出典と根拠

ORDレコード
ord-fc54f258afe5475a87923796414271bb
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09006229B2

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