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1,2-Dichloroethane → HCID 69932959、化合物

HRID 540796
ノート
印刷プレビュー

反応式

HRID 540796 の反応式
[F:1][C:2]([F:38])([F:37])[C:3]1[CH:36]=[CH:35][C:6]([O:7][C:8]2[N:12]([CH2:13][C:14](O)=[O:15])[N:11]=[C:10]([C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([C:23]4([NH:27][C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29])[CH2:26][O:25][CH2:24]4)[CH:18]=3)[CH:9]=2)=[CH:5][CH:4]=1.Cl.[CH3:40][NH:41][CH3:42].C(Cl)CCl.C1C=CC2N(O)N=NC=2C=1.C(N(C(C)C)CC)(C)C>CN(C=O)C.CCOC(C)=O>[F:38][C:2]([F:1])([F:37])[C:3]1[CH:36]=[CH:35][C:6]([O:7][C:8]2[N:12]([CH2:13][C:14]([N:41]([CH3:42])[CH3:40])=[O:15])[N:11]=[C:10]([C:17]3[CH:18]=[C:19]([C:23]4([NH:27][C:28](=[O:29])[O:30][C:31]([CH3:32])([CH3:33])[CH3:34])[CH2:24][O:25][CH2:26]4)[CH:20]=[CH:21][CH:22]=3)[CH:9]=2)=[CH:5][CH:4]=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 5

HCID 111,2-DichloroethaneHCID 10473Dimethylamine, hydrochlorideHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 67111333HCID 67111333、化合物

生成物 1

HCID 69932959HCID 69932959、化合物

試薬・触媒・溶媒 2

HCID 6228
Dimethylformamide
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

[5-(4-Trifluoromethylphenoxy)-3-(3-{3-[(tert-butyloxycarbonyl)amino]oxetan-3-yl}phenyl)-1H-pyrazol-1-yl]acetic acid (85 mg, 0.16 mmol), dimethylamine hydrochloride (26 mg, 0.32 mmol), EDC (46 mg, 0.24 mmol), HOBT (37 mg, 0.24 mmol), and diisopropylethylamine (0.11 mL, 0.64 mmol) were combined in 0.5 mL of DMF and the mixture was stirred at ambient temperature for 18 h. The mixture was diluted with EtOAc and washed with water and brine. The organic phase was dried over MgSO4, filtered, and the solvent was removed under reduced pressure. The residue was chromatographed on a 12 g silica gel column using 0-5% MeOH:CHCl3 over 15 min at 30 mL/min. Product-containing fractions were combined and the solvents were evaporated under reduced pressure to give tert-butyl [3-(3-{5-(4-trifluoromethylphenoxy)-1-[2-(dimethylamino)-2-oxoethyl]-1H-pyrazol-3-yl}phenyl)oxetan-3-yl]carbamate as a foam. Calcd (M+1)+: 561.6. Found: 561.0

後処理

  1. washwashed with water and brine
  2. dry with materialThe organic phase was dried over MgSO4
  3. filtrationfiltered
  4. customthe solvent was removed under reduced pressure
  5. customThe residue was chromatographed on a 12 g silica gel column
  6. waitCHCl3 over 15 min at 30 mL/min
  7. customthe solvents were evaporated under reduced pressure

出典と根拠

ORDレコード
ord-d754bcbfaf3e4cd4be3c72fcc25763ce
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08871796B2

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