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Thioglycolic Acid → (R)-6-(3-isopropyl-1-methyl-1H-pyrazol-5-yl)-2-(3-methyl-1-tosyl-1H-indol-4-yl)-4-(3-methylpiperazin-1-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine

HRID 80810
ノート
印刷プレビュー

反応式

HRID 80810 の反応式
[CH:1]([C:4]1[CH:8]=[C:7]([N:9]2[CH2:57][CH2:56][C:12]3[N:13]=[C:14]([C:36]4[CH:44]=[CH:43][CH:42]=[C:41]5[C:37]=4[C:38]([CH3:55])=[CH:39][N:40]5[S:45]([C:48]4[CH:54]=[CH:53][C:51]([CH3:52])=[CH:50][CH:49]=4)(=[O:47])=[O:46])[N:15]=[C:16]([N:17]4[CH2:22][CH2:21][N:20](S(C5C=CC=CC=5[N+]([O-])=O)(=O)=O)[C@H:19]([CH3:35])[CH2:18]4)[C:11]=3[CH2:10]2)[N:6]([CH3:58])[N:5]=1)([CH3:3])[CH3:2].C1CCN2C(=NCCC2)CC1.SCC(O)=O>CN(C=O)C.O.ClCCl>[CH:1]([C:4]1[CH:8]=[C:7]([N:9]2[CH2:57][CH2:56][C:12]3[N:13]=[C:14]([C:36]4[CH:44]=[CH:43][CH:42]=[C:41]5[C:37]=4[C:38]([CH3:55])=[CH:39][N:40]5[S:45]([C:48]4[CH:49]=[CH:50][C:51]([CH3:52])=[CH:53][CH:54]=4)(=[O:46])=[O:47])[N:15]=[C:16]([N:17]4[CH2:22][CH2:21][NH:20][C@H:19]([CH3:35])[CH2:18]4)[C:11]=3[CH2:10]2)[N:6]([CH3:58])[N:5]=1)([CH3:2])[CH3:3]
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 3

HCID 1133Thioglycolic AcidHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 71240484HCID 71240484、化合物

生成物 1

HCID 71240581(R)-6-(3-isopropyl-1-methyl-1H-pyrazol-5-yl)-2-(3-methyl-1-tosyl-1H-indol-4-yl)-4-(3-methylpiperazin-1-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine

試薬・触媒・溶媒 3

HCID 962Water
溶媒
HCID 6228Dimethylformamide溶媒
HCID 6344Dichloromethane溶媒

実験手順

To a solution of (R)-6-(3-isopropyl-1-methyl-1H-pyrazol-5-yl)-2-(3-methyl-1-tosyl-1H-indol-4-yl)-4-(3-methyl-4-((2-nitrophenyl)sulfonyl)piperazin-1-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine (105 mg, 0.127 mmol) in DMF (3 mL) was added DBU (0.1 mL, 0.64 mmol) followed by 2-mercaptoacetic acid (0.018 mL, 0.255 mmol). The mixture was stirred for 3 hours and then diluted with water and dichloromethane. The layers were separated and the aqueous layer was extracted three additional times with dichloromethane. The organic layers were combined, dried over Na2SO4, filtered and concentrated. The resulting residue was purified via silica gel flash chromatography [4-25% (2 M NH3 in MeOH)/DCM] to provide (R)-6-(3-isopropyl-1-methyl-1H-pyrazol-5-yl)-2-(3-methyl-1-tosyl-1H-indol-4-yl)-4-(3-methylpiperazin-1-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine. MS (ESI+) m/z 639.4 (M+H)+.

後処理

  1. customThe layers were separated
  2. extractionthe aqueous layer was extracted three additional times with dichloromethane
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe resulting residue was purified via silica gel flash chromatography [4-25% (2 M NH3 in MeOH)/DCM]

出典と根拠

ORDレコード
ord-df0755466f0540289aa0b3a87923e88c
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08846656B2

反応ノート

読み込み中…

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