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Sodium triacetoxyborohydride → 2-Diphenylmethyl-3-[(2-methoxy-5-(methylethyl)phenyl)methylamino]-4-(2-dimethylaminocarbamoyl-ethyl)pyrrolidine

HRID 1451493
ノート
印刷プレビュー

反応式

HRID 1451493 の反応式
[C:1]1([CH:7]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH:8]2[CH:12]([NH2:13])[CH:11]([CH2:14][CH2:15][C:16](=[O:21])[NH:17][N:18]([CH3:20])[CH3:19])[CH2:10][NH:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:28][O:29][C:30]1[CH:37]=[CH:36][C:35]([CH:38]([CH3:40])[CH3:39])=[CH:34][C:31]=1[CH:32]=O.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClC(Cl)C>[C:22]1([CH:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[CH:8]2[CH:12]([NH:13][CH2:32][C:31]3[CH:34]=[C:35]([CH:38]([CH3:40])[CH3:39])[CH:36]=[CH:37][C:30]=3[O:29][CH3:28])[CH:11]([CH2:14][CH2:15][C:16](=[O:21])[NH:17][N:18]([CH3:20])[CH3:19])[CH2:10][NH:9]2)[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 5049666Sodium triacetoxyborohydrideHCID 70095025-Isopropyl-2-methoxybenzaldehydeHCID 67694043HCID 67694043、化合物

生成物 1

HCID 200880122-Diphenylmethyl-3-[(2-methoxy-5-(methylethyl)phenyl)methylamino]-4-(2-dimethylaminocarbamoyl-ethyl)pyrrolidine収率 62%

試薬・触媒・溶媒 1

HCID 63651,1-Dichloroethane
溶媒

実験手順

A solution of 100 mg (0.272 mmol) [(2SR, 3SR, 4RS)-2-diphenylmethyl-3-amino-4-(2-dimethylaminocarbamoylethyl)pyrrolidine](the product of Example 26B) in 25 ml of dichloroethane was treated with 48 mg (0.272 mmol) of 2-methoxy-5isopropylbenzaldehyde and 81 mg (0.381 mmol) of sodium triacetoxyborohydride. The reaction mixture was stirred for 18 hours and then quenched with 15 ml of saturated aqueous sodium bicarbonate. The reaction mixture was extracted with methylene chloride and the organic phase was washed with brine, dried and evaporated. The residue was chromatographed on silica gel eluting with 97/2/1 (methylene chloride/methanol/ammonia) to afford 89 mg (62%) of the title compound.

後処理

  1. customquenched with 15 ml of saturated aqueous sodium bicarbonate
  2. extractionThe reaction mixture was extracted with methylene chloride
  3. washthe organic phase was washed with brine
  4. customdried
  5. customevaporated
  6. customThe residue was chromatographed on silica gel eluting with 97/2/1 (methylene chloride/methanol/ammonia)

出典と根拠

ORDレコード
ord-c7681c6b7cd9480e82a475df99bd3bb4
出典データセット
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05604252

反応ノート

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