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Triphenylphosphine → HCID 86612918、化合物

HRID 2422360
ノート
印刷プレビュー

反応式

HRID 2422360 の反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC(OC(/N=N/C(OC(C)C)=O)=O)C.[F:34][C:35]([F:46])([F:45])[C:36]([NH:38][C:39]1[CH:43]=[CH:42][S:41][C:40]=1[I:44])=[O:37].[C:47]([O:51][C:52]([N:54]1[CH2:59][CH:58]=[C:57]([CH2:60]O)[CH2:56][CH2:55]1)=[O:53])([CH3:50])([CH3:49])[CH3:48]>O1CCCC1>[C:47]([O:51][C:52]([N:54]1[CH2:55][CH:56]=[C:57]([CH2:60][N:38]([C:39]2[CH:43]=[CH:42][S:41][C:40]=2[I:44])[C:36](=[O:37])[C:35]([F:34])([F:45])[F:46])[CH2:58][CH2:59]1)=[O:53])([CH3:50])([CH3:48])[CH3:49]
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 4

HCID 11776TriphenylphosphineHCID 5363146Diisopropyl azodicarboxylateHCID 225944841,1-Dimethylethyl 3,6-dihydro-4-(hydroxymethyl)-1(2H)-pyridinecarboxylateHCID 588961652,2,2-Trifluoro-N-(2-iodothiophen-3-yl)acetamide

生成物 1

HCID 86612918HCID 86612918、化合物収率 62.9%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒
3 回

反応条件

温度
-10 °C

実験手順

Triphenylphosphine (2.29 g) was dissolved in tetrahydrofuran (50 ml) and the solution was cooled to −10° C. under argon. Diisopropylazodicarboxylate (1.70 ml) was added dropwise over 10 min and the resulting mixture was stirred at −10° C. for 20 min (formation of a white precipitate). 2,2,2-Trifluoro-N-(2-iodo-thiophen-3-yl)-acetamide (2.25 g) dissolved in a minimum volume of tetrahydrofuran was added, followed by 4-Hydroxymethyl-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (J. Org. Chem. 2001, 66, 5545-5551, 1.49 g) dissolved in a minimum volume of tetrahydrofuran. The reaction mixture was allowed to warm to room temperature and stirred for 12 hours. The solution was then concentrated in vacuo and the residue subjected to silica gel chromatography (cyclohexane:ethyl acetate 93:7) to afford 4-{[(2-Iodo-thiophen-3-yl)-(2,2,2-trifluoro-acetyl)-amino]-methyl}-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester as a colourless oil (2.27 g). 1H NMR (400 MHz, CDCl3) 1.5 (s, 9H), 2.15 (m, 2H), 3.43 (m, 1H), 3.52 (m 1H), 3.75 (d, J=19 Hz, 1H), 3.77 (m, 2H), 4.76 (d, J=17 Hz, 1H), 5.41 (s, 1H), 6.68 (br d, J=5.5 Hz, 1H), 7.42 (d, J=5.5 Hz, 1H); MS (ES+) 417 (M+H+—CO2-isobutene), 458 (M+H+-isobutene).

後処理

  1. additionwas added
  2. temperatureto warm to room temperature
  3. stirringstirred for 12 hours
  4. concentrationThe solution was then concentrated in vacuo

出典と根拠

ORDレコード
ord-09faa6974126477da963b80ca1b4448f
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07960401B2

反応ノート

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