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Dicyclohexylcarbodiimide → HCID 59401183、化合物

HRID 1255092
ノート
印刷プレビュー

反応式

HRID 1255092 の反応式
Cl.[F:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH:9]([NH:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:10]([OH:12])=[O:11].[N:20]12[CH2:27][CH2:26][CH:23]([CH2:24][CH2:25]1)[C@@H:22](O)[CH2:21]2.N1(O)C2C=CC=CC=2N=N1.C1CCC(N=C=NC2CCCCC2)CC1>C1COCC1>[N:20]12[CH2:27][CH2:26][CH:23]([CH2:24][CH2:25]1)[C@@H:22]([O:11][C:10](=[O:12])[CH:9]([C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=1[F:2])[NH:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH2:21]2
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 10868Dicyclohexylcarbodiimide2 回HCID 757711-HydroxybenzotriazoleHCID 914043-Quinuclidinol, (-)-2 回HCID 67425668(2-Fluoro-phenyl)-phenylamino-acetic acid hydrochloride

生成物 1

HCID 59401183HCID 59401183、化合物収率 82.4%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

実験手順

To a solution of (2-fluoro-phenyl)-phenylamino-acetic acid hydrochloride (I261) (217 mg, 0.77 mmol), (R)-quinuclidin-3-ol (338 mg, 2.66 mmol) and 1H-benzo[d][1,2,3]triazol-1-ol (180 mg, 1.332 mmol) in dry THF (15 mL), is added PS-DCC (1.0 g, 1.33 mmol). The mixture is shaken at RT for 15 hours. Then (R)-quinuclidin-3-ol (49.0 mg, 0.38 mmol) and PS-DCC (290 mg, 0.38 mmol) are added again and the reaction is shaken for additional 3 hours at RT. The resin is removed by filtration and washed several time with EtOAc. The solvent is evaporated, the residue is taken up with EtOAc and washed with NaHCO3, water and brine. The organic phase is dried (Na2SO4), filtered and evaporated to afford the title compound as a brown oil (225 mg, 82% yield).

後処理

  1. stirringthe reaction is shaken for additional 3 hours at RT
  2. customThe resin is removed by filtration
  3. washwashed several time with EtOAc
  4. customThe solvent is evaporated
  5. washwashed with NaHCO3, water and brine
  6. dry with materialThe organic phase is dried (Na2SO4)
  7. filtrationfiltered
  8. customevaporated

出典と根拠

ORDレコード
ord-2c81f1889ca24cdfa8f2f0019174a8de
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08455646B2

反応ノート

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