Triethylamine → 3'-chloro-4-(1-ethyl-5-methyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl

HRID 220553ノート

反応式

HRID 220553 の反応式
[CH2:1]([N:3]1[C:7]([CH3:8])=[C:6]([CH:9]=O)[CH:5]=[N:4]1)[CH3:2].Cl.Cl.[Cl:13][C:14]1[C:15]([N:20]2[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]2)=[N:16][CH:17]=[CH:18][N:19]=1.C(N(CC)CC)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCCl.C(O)(=O)C>[Cl:13][C:14]1[C:15]([N:20]2[CH2:21][CH2:22][N:23]([CH2:9][C:6]3[CH:5]=[N:4][N:3]([CH2:1][CH3:2])[C:7]=3[CH3:8])[CH2:24][CH2:25]2)=[N:16][CH:17]=[CH:18][N:19]=1

参加物

7

実験手順

Dissolve 1-ethyl-5-methyl-1H-pyrazole-4-carbaldehyde (2.92 g, 21.1 mmol) in 1,2-dichloroethane (184 mL). Add 3′-chloro-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl dihydrochloride (4.97 g, 18.3 mmol), triethylamine (5.9 mL, 42.3 mmol), sodium triacetoxyborohydride (6.72 g, 31.7 mmol) and acetic acid (1.98 mL) and stir at room temperature for 18 hr. Add aq. saturated sodium bicarbonate and extract four times with DCM. Dry combined organic layers (magnesium sulfate), filter, concentrate, and purify (silica gel chromatography, eluting with 50:50 to 100:0 ethyl acetate:hexanes then 10:90 to 20:80 methanol:ethyl acetate) to give 3′-chloro-4-(1-ethyl-5-methyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (5.2 g, 88%). MS (ES): m/z=321 [M+H]+.

後処理

  1. extractionAdd aq. saturated sodium bicarbonate and extract four times with DCM
  2. customDry
  3. filtrationfilter
  4. concentrationconcentrate
  5. custompurify (silica gel chromatography
  6. washeluting with 50:50 to 100:0 ethyl acetate

出典と根拠

ORDレコード
ord-8001cda7f8dd4de2aa89f2d9acdb9526
出典データセット
uspto-grants-2012_06
特許番号
US08202873B2

反応ノート

読み込み中…