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4-Methylmorpholine → (+/-)-3-{4-[2-Cyclohexyl-1-(4'-trifluoromethyl-biphenyl-4-yl)-ethoxy]-3-methyl-benzoylamino}-2-methyl-propionic acid ethyl ester

HRID 1669277
ノート
印刷プレビュー

反応式

HRID 1669277 の反応式
[CH:1]1([CH2:7][CH:8]([C:19]2[CH:24]=[CH:23][C:22]([C:25]3[CH:30]=[CH:29][C:28]([C:31]([F:34])([F:33])[F:32])=[CH:27][CH:26]=3)=[CH:21][CH:20]=2)[O:9][C:10]2[CH:18]=[CH:17][C:13](C(O)=O)=[CH:12][CH:11]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Cl[C:36]1[N:41]=[C:40]([O:42]C)N=C(OC)N=1.[CH3:46]N1CCOCC1.[CH2:53]([O:55][C:56](=[O:61])[CH:57](O)[CH2:58]N)[CH3:54]>C1COCC1.CCOC(C)=O.O>[CH2:53]([O:55][C:56](=[O:61])[CH:57]([CH3:58])[CH2:36][NH:41][C:40](=[O:42])[C:13]1[CH:12]=[CH:11][C:10]([O:9][CH:8]([C:19]2[CH:24]=[CH:23][C:22]([C:25]3[CH:30]=[CH:29][C:28]([C:31]([F:34])([F:33])[F:32])=[CH:27][CH:26]=3)=[CH:21][CH:20]=2)[CH2:7][CH:1]2[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]2)=[C:18]([CH3:46])[CH:17]=1)[CH3:54]
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 4

HCID 79724-Methylmorpholine2 回HCID 184502-Chloro-4,6-dimethoxy-1,3,5-triazineHCID 21834752Ethyl 3-amino-2-hydroxypropanoateHCID 59729441(+/-)-4-[2-Cyclohexyl-1-(4'-trifluoromethyl-biphenyl-4-yl)-ethoxy]-benzoic acid

生成物 1

HCID 67341724(+/-)-3-{4-[2-Cyclohexyl-1-(4'-trifluoromethyl-biphenyl-4-yl)-ethoxy]-3-methyl-benzoylamino}-2-methyl-propionic acid ethyl ester
収率 56%

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒HCID 8857Ethyl Acetate溶媒

実験手順

A solution of (±)-4-[2-cyclohexyl-1-(4′-trifluoromethyl-biphenyl-4-yl)-ethoxy]-benzoic acid (0.0813 g, 0.174 mmol) in THF (1.7 mL) is treated with 2-chloro-4,6-dimethoxy-[1,3,5]triazine (CDMT, 0.0338 g, 0.193 mmol) and N-methyl morpholine (NMM, 0.020 mL, 0.27 mmol). The mixture is added to a flask containing (±)-3-amino-2-hydroxy-propionic acid ethyl ester (0.0465 g, 0.274 mmol). Additional NMM (0.030 mL, 0.273 mmol) and H2O (0.4 mL) are added and the reaction is stirred overnight. The reaction mixture is dissolved in EtOAc (10 mL) and washed with 0.1 N HCl (2×10 mL), ph=7 phosphate buffer (1×), brine (1×), dried over MgSO4, filtered, and conc. The residue is loaded onto silica gel and eluted with hexanes using a gradient of 10% EtOAc to 60% EtOAc giving (±)-3-{4-[2-cyclohexyl-1-(4′-trifluoromethyl-biphenyl-4-yl)-ethoxy]-3-methyl-benzoylamino}-2-methyl-propionic acid ethyl ester (0.0568 g, 56%) as a white foam. MS (ES): 582.3 [M−H]−.

後処理

  1. additionThe mixture is added to a flask
  2. washwashed with 0.1 N HCl (2×10 mL), ph=7 phosphate buffer (1×), brine (1×)
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. washeluted with hexanes using a gradient of 10% EtOAc to 60% EtOAc

出典と根拠

ORDレコード
ord-6db01be673ce4679b78a68fb5dfa4e1f
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07989457B2

反応ノート

読み込み中…

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