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Formaldehyde → tert-butyl (6S,7S)-5-methyl-6-{[4-(3-methylphenyl)piperazin-1-yl]carbonyl}-5-azaspiro[2.5]octane-7-carboxylate

HRID 2240493
ノート
印刷プレビュー

反応式

HRID 2240493 の反応式
[C:1]([O:5][C:6]([C@H:8]1[CH2:15][C:12]2([CH2:14][CH2:13]2)[CH2:11][NH:10][C@@H:9]1[C:16]([OH:18])=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=C[C:29]=2N=N1.[CH3:46][C:47]1[CH:48]=[C:49]([N:53]2[CH2:58][CH2:57][NH:56][CH2:55][CH2:54]2)[CH:50]=[CH:51][CH:52]=1.C(N(C(C)C)CC)(C)C.C=O.[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+]>CN(C=O)C>[CH3:29][N:10]1[C@H:9]([C:16]([N:56]2[CH2:57][CH2:58][N:53]([C:49]3[CH:50]=[CH:51][CH:52]=[C:47]([CH3:46])[CH:48]=3)[CH2:54][CH2:55]2)=[O:18])[C@@H:8]([C:6]([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:7])[CH2:15][C:12]2([CH2:13][CH2:14]2)[CH2:11]1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 6

HCID 712FormaldehydeHCID 81531DiisopropylethylamineHCID 831111-(m-Tolyl)piperazineHCID 151348Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 5049666Sodium triacetoxyborohydrideHCID 16108946HCID 16108946、化合物

生成物 1

HCID 67438575
tert-butyl (6S,7S)-5-methyl-6-{[4-(3-methylphenyl)piperazin-1-yl]carbonyl}-5-azaspiro[2.5]octane-7-carboxylate

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A mixture of (6S,7S)-7-(tert-butoxycarbonyl)-5-azaspiro[2.5]octane-6-carboxylic acid of step 1 g (25 mg), BOP (45 mg), 1-(3-methylphenyl)piperazine (176 mg) and di-isopropylethylamine (70 μL) in DMF (500 μL) was stirred at RT overnight. Formaldehyde solution (0.5 M in THF/MeCN (1:1), 600 μL) was added to the mixture followed by NaBH(OAc)3 (0.25 M in THF/MeCN (1:1), 1000 μL). The resulting mixture was stirred overnight. The solvents were removed under reduced pressure. The residue was dissolved in ethyl acetate (5 mL). The solution was washed with NaHCO3 (7.5%, 3×1 mL). The organic phase was dried over MgSO4 and filtered and concentrated. The residue was used directly in the next step reaction without further purification.

後処理

  1. stirringThe resulting mixture was stirred overnight
  2. customThe solvents were removed under reduced pressure
  3. dissolutionThe residue was dissolved in ethyl acetate (5 mL)
  4. washThe solution was washed with NaHCO3 (7.5%, 3×1 mL)
  5. dry with materialThe organic phase was dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was used directly in the next step reaction without further purification

出典と根拠

ORDレコード
ord-b26f33ea35b844eca492d9ddc698392c
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07723349B2

反応ノート

読み込み中…

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