Sodium borohydride → (2S)-2-(tert-butoxycarbonylamino)-5-(5,6,7,8-tetrahydroquinolin-8-ylamino)-pentanoic acid tert-butyl ester

HRID 899615

反応式

HRID 899615 の反応式
[C:1]([O:5][C:6](=[O:20])[C@@H:7]([NH:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:8][CH2:9][CH2:10][NH2:11])([CH3:4])([CH3:3])[CH3:2].[N:21]1[C:30]2[C:29](=O)[CH2:28][CH2:27][CH2:26][C:25]=2[CH:24]=[CH:23][CH:22]=1.[BH4-].[Na+]>CO>[C:1]([O:5][C:6](=[O:20])[C@@H:7]([NH:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:8][CH2:9][CH2:10][NH:11][CH:29]1[C:30]2[N:21]=[CH:22][CH:23]=[CH:24][C:25]=2[CH2:26][CH2:27][CH2:28]1)([CH3:4])([CH3:3])[CH3:2]

参加物

5

反応物 3

HCID 4311764Sodium borohydrideHCID 7006667(S)-tert-Butyl 5-amino-2-((tert-butoxycarbonyl)amino)pentanoateHCID 117447776,7-Dihydro-5H-quinoline-8-one

生成物 1

HCID 69157433(2S)-2-(tert-butoxycarbonylamino)-5-(5,6,7,8-tetrahydroquinolin-8-ylamino)-pentanoic acid tert-butyl ester収率 54%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of (2S)-5-amino-2-(tert-butoxycarbonylamino)-pentanoic acid tert-butyl ester (free base) (0.905 g, 3.11 mmol) in CH3OH (15 mL) was added 6,7-dihydro-5H-quinolin-8-one (0.504 g, 3.43 mmol) and the resultant solution was stirred at room temperature for 5 hours. Powdered NaBH4 (0.379 g, 9.98 mmol) was added, and the mixture was stirred at room temperature for 25 minutes then concentrated under reduced pressure. The residue was dissolved in CH2Cl2 (100 mL) and brine (20 mL). The phases were separated and the aqueous phase was extracted with CH2Cl2 (3×20 mL). The combined organic extracts were dried (Na2SO4) and concentrated. Purification of the crude material by column chromatography on silica gel (20:1 CH2Cl2—CH3OH) provided 0.700 g (54%) of (2S)-2-tert-butoxycarbonylamino-5-(5,6,7,8-tetrahydroquinolin-8-ylamino)-pentanoic acid tert-butyl ester as a yellow oil.

後処理

  1. concentrationthen concentrated under reduced pressure
  2. dissolutionThe residue was dissolved in CH2Cl2 (100 mL)
  3. customThe phases were separated
  4. extractionthe aqueous phase was extracted with CH2Cl2 (3×20 mL)
  5. dry with materialThe combined organic extracts were dried (Na2SO4)
  6. concentrationconcentrated
  7. customPurification of the crude material by column chromatography on silica gel (20:1 CH2Cl2—CH3OH)

出典と根拠

ORDレコード
ord-249cbc6b535248f5888482ade88491cf
出典データセット
uspto-grants-2008_04
特許番号
US07354932B2

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