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2,6-Dimethylbenzoic acid → 2,6-Dimethyl-N-[[1-(methylamino)cyclopentyl](phenyl)methyl]benzamide

HRID 20844
ノート
印刷プレビュー

反応式

HRID 20844 の反応式
[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:3]=1[C:4]([OH:6])=O.[NH2:12][CH:13]([C:20]1(CN)[CH2:24][CH2:23][CH2:22][CH2:21]1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.[CH3:27][N:28](C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>CN(C=O)C.CCN(C(C)C)C(C)C>[CH3:11][C:7]1[CH:8]=[CH:9][CH:10]=[C:2]([CH3:1])[C:3]=1[C:4]([NH:12][CH:13]([C:20]1([NH:28][CH3:27])[CH2:21][CH2:22][CH2:23][CH2:24]1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)=[O:6]
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 3

HCID 124392,6-Dimethylbenzoic acidHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 57444874{[Amino(phenyl)methyl]cyclopentyl}methylamine

生成物 1

HCID 115228862,6-Dimethyl-N-[[1-(methylamino)cyclopentyl](phenyl)methyl]benzamide収率 76%

試薬・触媒・溶媒 2

HCID 6228
Dimethylformamide
溶媒
HCID 81531Diisopropylethylamine溶媒

実験手順

To a solution of 2,6-dimethylbenzoic acid (0.100 g; 0.668 mmol) in DMF (5 ml) and DIPEA (0.12 ml) was added {[amino(phenyl)methyl]cyclopentyl}methylamine D31 enantiomer 2 (0.124 g; 0.608 mmol) and HATU (0.254 g; 0.668 mmol). The resulting mixture was allowed to stir at room temperature for 3 days and then the DMF was evaporated off under reduced pressure. Residual material was partitioned between ethyl acetate and water, washed with water and the organic layer was dried (Na2SO4) and evaporated. The residual material was dissolved in DCM (2 ml) and loaded onto an SCX cartridge. Washing with DCM, then methanol followed by elution with 1 M ammonia in methanol afforded the title product (155 mg; 76%). 1H NMR (CDCl3) δ: 1.3-1.8 (9H, m), 2.21 (3H, s), 2.28 (6H, s), 5.07 (1H, m), 7.0 (2H, m), 7.1-7.4 (7H, m). Mass Spectrum (Electrospray LC/MS). Found 337 (MH+). C22H28N2O requires 336. Ret. time: 1.86 min.

後処理

  1. customthe DMF was evaporated off under reduced pressure
  2. customResidual material was partitioned between ethyl acetate and water
  3. washwashed with water
  4. dry with materialthe organic layer was dried (Na2SO4)
  5. customevaporated
  6. dissolutionThe residual material was dissolved in DCM (2 ml)
  7. washWashing with DCM
  8. washmethanol followed by elution with 1 M ammonia in methanol

出典と根拠

ORDレコード
ord-4d7b6c3ca3c241229878f9f0254ed117
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07745642B2

反応ノート

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