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Triethylamine → N-(2-{[(3R)-1-(5-Hydroxy-5-pyridin-3-ylbicyclo[2.2.2]oct-2-yl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamide

HRID 1016083
ノート
印刷プレビュー

反応式

HRID 1016083 の反応式
Cl.[O:2]=[C:3]([NH:18][C@@H:19]1[CH2:23][CH2:22][NH:21][CH2:20]1)[CH2:4][NH:5][C:6](=[O:17])[C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([C:13]([F:16])([F:15])[F:14])[CH:8]=1.[OH:24][C:25]1([C:34]2[CH:35]=[N:36][CH:37]=[CH:38][CH:39]=2)[CH2:30][CH:29]2[CH2:31][CH2:32][CH:26]1[CH2:27][C:28]2=O.C(N(CC)CC)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C1COCC1>[OH:24][C:25]1([C:34]2[CH:35]=[N:36][CH:37]=[CH:38][CH:39]=2)[CH2:30][CH:29]2[CH2:31][CH2:32][CH:26]1[CH2:27][CH:28]2[N:21]1[CH2:22][CH2:23][C@@H:19]([NH:18][C:3](=[O:2])[CH2:4][NH:5][C:6](=[O:17])[C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([C:13]([F:15])([F:16])[F:14])[CH:8]=2)[CH2:20]1
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 8471TriethylamineHCID 5049666Sodium triacetoxyborohydrideHCID 595560585-Hydroxy-5-pyridin-3-ylbicyclo[2.2.2]octan-2-oneHCID 66787629N-{2-Oxo-2-[(3R)-pyrrolidin-3-ylamino]ethyl}-3-(trifluoromethyl)benzamide hydrochloride

生成物 1

HCID 59556078N-(2-{[(3R)-1-(5-Hydroxy-5-pyridin-3-ylbicyclo[2.2.2]oct-2-yl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamide

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

N-{2-Oxo-2-[(3R)-pyrrolidin-3-ylamino]ethyl}-3-(trifluoromethyl)benzamide hydrochloride (100 mg, 0.284 mmol) and 5-hydroxy-5-pyridin-3-ylbicyclo[2.2.2]octan-2-one (62.0 mg, 0.284 mmol) were dissolved in dry THF (10 mL). Triethylamine (80 uL, 0.57 mmol) and sodium triacetoxyborohydride (120 mg, 0.57 mmol) were added and the mixture was stirred at room temperature overnight. TLC indicated conversion to desired products in about a 1:1 ratio of isomers. Adsorbed reaction mixture onto silica gel and chromatographed eluting with dichloromethane to 10% methanol/dichloromethane/0.5% ammonium hydroxide. Fractions were combined to give pure higher Rf isomer and pure lower Rf isomer: Higher Rf product: LC/MS (positive ion) m/z=517.1 (M+H)+; Lower Rf product: LC/MS (positive ion) m/z=517.2 (M+H)+.

後処理

  1. customAdsorbed reaction mixture onto silica gel
  2. customchromatographed
  3. washeluting with dichloromethane to 10% methanol/dichloromethane/0.5% ammonium hydroxide
  4. customto give pure higher Rf isomer and pure lower Rf isomer

出典と根拠

ORDレコード
ord-15ff3d8e2d2f44b7ae2e2c559099b2b1
出典データセット
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07985730B2

反応ノート

読み込み中…

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