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Formaldehyde → N-[(3'-{[(3S)-3,4-dimethyl-1-piperazinyl]methyl}-6-fluoro-3-biphenylyl)methyl]-3-[(1-methyl-4-piperidinyl)methyl]benzamide

HRID 2080327
ノート
印刷プレビュー

反応式

HRID 2080327 の反応式
[CH3:1][C@@H:2]1[N:7]([CH3:8])[CH2:6][CH2:5][N:4]([CH2:9][C:10]2[CH:11]=[C:12]([C:16]3[C:21]([F:22])=[CH:20][CH:19]=[C:18]([CH2:23][NH:24][C:25](=[O:39])[C:26]4[CH:31]=[CH:30][CH:29]=[C:28]([CH2:32][CH:33]5[CH2:38][CH2:37][NH:36][CH2:35][CH2:34]5)[CH:27]=4)[CH:17]=3)[CH:13]=[CH:14][CH:15]=2)[CH2:3]1.[CH2:40]=O.[BH4-].[Na+]>CO>[CH3:1][C@@H:2]1[N:7]([CH3:8])[CH2:6][CH2:5][N:4]([CH2:9][C:10]2[CH:11]=[C:12]([C:16]3[C:21]([F:22])=[CH:20][CH:19]=[C:18]([CH2:23][NH:24][C:25](=[O:39])[C:26]4[CH:31]=[CH:30][CH:29]=[C:28]([CH2:32][CH:33]5[CH2:34][CH2:35][N:36]([CH3:40])[CH2:37][CH2:38]5)[CH:27]=4)[CH:17]=3)[CH:13]=[CH:14][CH:15]=2)[CH2:3]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 712FormaldehydeHCID 4311764Sodium borohydrideHCID 11706395N-[(3'-{[(3S)-3,4-dimethyl-1-piperazinyl]methyl}-6-fluoro-3-biphenylyl)methyl]-3-(4-piperidinylmethyl)benzamide

生成物 1

HCID 11656788N-[(3'-{[(3S)-3,4-dimethyl-1-piperazinyl]methyl}-6-fluoro-3-biphenylyl)methyl]-3-[(1-methyl-4-piperidinyl)methyl]benzamide収率 35.3%

試薬・触媒・溶媒 1

HCID 887
Methanol
溶媒

実験手順

To a solution of N-[(3′-{[(3S)-3,4-dimethyl-1-piperazinyl]methyl}-6-fluoro-3-biphenylyl)methyl]-3-(4-piperidinylmethyl)benzamide (165 mg, 0.313 mmol) in 3 mL of MeOH, was added dropwise formaldehyde (37%, 101 mg, 1.25 mmol). After stirring for 30 minutes, sodium borohydride (24 mg, 0.63 mmol) was added. After stirring of the resulting mixture at rt for 12 hours, the solvent was removed under vacuum and the residue was purified by loading onto a 2 g aminopropyl SPE cartridge and eluting sequentially with DCM (3×5 mL), EtOAc (3×5 mL), and MeOH (3×5 mL). The DCM factions were combined and evaporated to give the title compound as a white solid (60 mg, 35%). LC/MS: m/z, 543 (M+H), 1.18 min.

後処理

  1. stirringAfter stirring of the resulting mixture at rt for 12 hours
  2. customthe solvent was removed under vacuum
  3. customthe residue was purified
  4. washeluting sequentially with DCM (3×5 mL), EtOAc (3×5 mL), and MeOH (3×5 mL)
  5. customevaporated

出典と根拠

ORDレコード
ord-d1cac5328ce8403f803c5eb9a385e122
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07932247B2

反応ノート

読み込み中…

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