tert-Butyl methyl ether → 1-{4-[(S)-4-(2,3-Dihydro-[1,4]dioxino[2,3-b]pyridin-3-yl)-benzyl]-piperazin-1-yl}-2-hydroxy-ethanone

HRID 1842003ノート

反応式

HRID 1842003 の反応式
[N:1]1([CH2:7][C:8]2[CH:13]=[CH:12][C:11]([C@@H:14]3[O:23][C:18]4=[N:19][CH:20]=[CH:21][CH:22]=[C:17]4[O:16][CH2:15]3)=[CH:10][CH:9]=2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.Cl[C:25]([CH2:27][O:28]C(=O)C)=[O:26].CCN(C(C)C)C(C)C.C(OC)(C)(C)C>C(Cl)Cl>[O:16]1[C:17]2[C:18](=[N:19][CH:20]=[CH:21][CH:22]=2)[O:23][C@@H:14]([C:11]2[CH:12]=[CH:13][C:8]([CH2:7][N:1]3[CH2:6][CH2:5][N:4]([C:25](=[O:26])[CH2:27][OH:28])[CH2:3][CH2:2]3)=[CH:9][CH:10]=2)[CH2:15]1

参加物

6

反応物 4

HCID 15413tert-Butyl methyl etherHCID 26297Acetoxyacetyl chlorideHCID 81531DiisopropylethylamineHCID 86695358(S)-3-(4-piperazin-1-ylmethyl-phenyl)-2,3-dihydro-[1,4]dioxino[2,3-b]pyridine

生成物 1

HCID 717371781-{4-[(S)-4-(2,3-Dihydro-[1,4]dioxino[2,3-b]pyridin-3-yl)-benzyl]-piperazin-1-yl}-2-hydroxy-ethanone

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of Intermediate S (5.80 g, 17.7 mmol) in DCM (200 mL) at 0° C. is added acetic acid chlorocarbonylmethyl ester (2.16 mL, 19.5 mmol) followed by DIPEA (7.50 mL, 35.4 mmol) and the mixture stirred at rt for 1 h. The reaction was concentrated and the residue dissolved in 4:1 MeOH/water (100 mL) then treated with LiOH monohydrate (2.23 g, 53.1 mmol). After 72 h, the reaction is poured into ice water and the resulting solid isolated by filtration. The solid is suspended in refluxing tert-butylmethyl ether (400 mL) for 20 min and the remaining undissolved material separated out by filtration. The cooled filtrate produces a solid that is then isolated by filtration in several crops. The undissolved material from the first filtration is dissolved in refluxing 1,4-dioxane and cooled to give an additional crop of solid. The crops are combined to give the title product 253. (LC/MS method 16: ES+ m/z 370.3 [M+H]+, Rt=0.35 min)

後処理

  1. concentrationThe reaction was concentrated
  2. dissolutionthe residue dissolved in 4:1 MeOH/water (100 mL)
  3. waitAfter 72 h
  4. customthe resulting solid isolated by filtration
  5. customthe remaining undissolved material separated out by filtration
  6. customThe cooled filtrate produces a solid
  7. customthat is then isolated by filtration in several crops
  8. filtrationThe undissolved material from the first filtration
  9. dissolutionis dissolved
  10. temperaturein refluxing 1,4-dioxane
  11. temperaturecooled
  12. customto give an additional crop of solid

出典と根拠

ORDレコード
ord-6578b04648d64e6cbd4a2bc1f91c6c42
出典データセット
uspto-grants-2015_02
特許番号
US08946203B2

反応ノート

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