ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Triethylamine → N-[[1-(Dimethylamino)cyclopentyl](phenyl)methyl]-2-methyl-4,6-bis(trifluoromethyl)benzamide

HRID 20852
ノート
印刷プレビュー

反応式

HRID 20852 の反応式
[CH3:1][C:2]1[CH:10]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:8]=[C:7]([C:15]([F:18])([F:17])[F:16])[C:3]=1[C:4](Cl)=[O:5].FC(F)(F)C1C=C(C(F)(F)F)C=CC=1C(OC)=O.[NH2:37][CH:38]([C:47]1[CH:52]=[CH:51][CH:50]=[CH:49][CH:48]=1)[C:39]1([N:44]([CH3:46])[CH3:45])[CH2:43][CH2:42][CH2:41][CH2:40]1.COC1C=C(C(F)(F)F)C=C(C(F)(F)F)C=1C(NC(C1C=CC=CC=1)C(C)(N1CCCC1)CC)=O.C(N(CC)CC)C>C(Cl)Cl>[CH3:45][N:44]([CH3:46])[C:39]1([CH:38]([C:47]2[CH:52]=[CH:51][CH:50]=[CH:49][CH:48]=2)[NH:37][C:4](=[O:5])[C:3]2[C:7]([C:15]([F:18])([F:17])[F:16])=[CH:8][C:9]([C:11]([F:14])([F:13])[F:12])=[CH:10][C:2]=2[CH3:1])[CH2:43][CH2:42][CH2:41][CH2:40]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 8471TriethylamineHCID 11521393{1-[Amino(phenyl)methyl]cyclopentyl}dimethylamineHCID 18925643Methyl 2,4-bis(trifluoromethyl)benzoateHCID 59347787HCID 59347787、化合物HCID 59347796(+/-)-2-(Methyloxy)-N-[2-methyl-1-phenyl-2-(1-pyrrolidinyl)butyl]-4,6-bis(trifluoromethyl)benzamide

生成物 1

HCID 59347766
N-[[1-(Dimethylamino)cyclopentyl](phenyl)methyl]-2-methyl-4,6-bis(trifluoromethyl)benzamide
収率 36%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A mixture of 2-methyl-4,6-bis(trifluoromethyl)benzoyl chloride and methyl 2,4-bis(trifluoromethyl)benzoate (approximately 0.5 mmol) prepared as described in D53 was dissolved in dry DCM (3 ml) and treated with (+)-{1-[amino(phenyl)methyl]cyclopentyl}dimethylamine D3 enantiomer 2 (109 mg, 0.50 mmol) and triethylamine (140 ul, 1.00 mmol) and left overnight at room temperature. The volatile components were removed under reduced pressure and the residue chromatographed on silica gel. Elution with 0-80% ethyl acetate in pentane gave the title product (86 mg, ca.36%). 1H NMR (CDCl3) δ: 0.95 (1H, br m), 1.44-1.86 (7H, overlapping m), 2.20 (6H, s), 2.41 (3H, br s), 5.10 (1H, d, J=5.6 Hz), 7.07 (1H, br s), 7.26-7.42 (5H, overlapping m), 7.67 (1H, s), 7.77 (1H, s). Mass Spectrum (Electrospray LC/MS): Found 473 (MH+) C24H26F6N2O requires 472. Ret time 2.25 min.

後処理

  1. customprepared
  2. customThe volatile components were removed under reduced pressure
  3. customthe residue chromatographed on silica gel
  4. washElution with 0-80% ethyl acetate in pentane

出典と根拠

ORDレコード
ord-393535b390e64c34ba1549506cc2f4d3
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

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート