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Diethyl Ether → HCID 70059617、化合物

HRID 2230292
ノート
印刷プレビュー

反応式

HRID 2230292 の反応式
[C:1]([NH:8][C@H:9]([C:27](O)=[O:28])[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:18][C:19]2[C:24]([Cl:25])=[CH:23][CH:22]=[CH:21][C:20]=2[Cl:26])=[CH:13][CH:12]=1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[C:54]([NH2:58])([CH3:57])([CH3:56])[CH3:55].CCOCC>CN(C=O)C.CCN(C(C)C)C(C)C>[C:4]([O:3][C:1](=[O:2])[NH:8][C@H:9]([C:27](=[O:28])[NH:58][C:54]([CH3:57])([CH3:56])[CH3:55])[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:18][C:19]2[C:24]([Cl:25])=[CH:23][CH:22]=[CH:21][C:20]=2[Cl:26])=[CH:13][CH:12]=1)([CH3:6])([CH3:5])[CH3:7]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 3283Diethyl EtherHCID 6385Tert-ButylamineHCID 2733084Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 11133964L-Tyrosine, O-[(2,6-dichlorophenyl)methyl]-N-[(1,1-dimethylethoxy)carbonyl]-

生成物 1

HCID 70059617HCID 70059617、化合物収率 69.4%

試薬・触媒・溶媒

2
HCID 6228Dimethylformamide溶媒HCID 81531Diisopropylethylamine溶媒

反応条件

温度
0 °C

実験手順

A solution of BOC-O-(2,6-dichlorobenzyl)-L-tyrosine (Bachem, 2.00 g, 4.54 mmol) in 20 mL of DMF and iPr2NEt (1.6 mL) was cooled to 0° C. and treated with HBTU (1.72 g, 4.54 mmol). The resulting solution was stirred at 0° C. for 30 minutes and treated with tert-butyl amine (0.48 mL, 4.54 mmol). The resulting solution was stirred overnight. The reaction mixture was poured into ether (100 mL) and washed sequentially with saturated aqueous NaHCO3 solution (20 mL) and brine (4×20 mL). The organic phase was collected and dried (MgSO4) and concentrated. The crude reaction product was purified by chromatography (silica gel, 2:1 heptane/EtOAc). The solid obtained was crystallized from hot heptane, collected by suction filtration and dried to give the title compound as a white solid (1.56 g, 69%), mp=82-86° C.

後処理

  1. stirringThe resulting solution was stirred overnight
  2. washwashed sequentially with saturated aqueous NaHCO3 solution (20 mL) and brine (4×20 mL)
  3. customThe organic phase was collected
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated
  6. customThe crude reaction product
  7. customwas purified by chromatography (silica gel, 2:1 heptane/EtOAc)
  8. customThe solid obtained
  9. customwas crystallized from hot heptane
  10. filtrationcollected by suction filtration
  11. customdried

出典と根拠

ORDレコード
ord-e0ea3705da364abbadc5e11464b48aa0
出典データセット
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06423689B1

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート