Sodium Hydroxide → HCID 67428977、化合物

HRID 1887091ノート

反応式

HRID 1887091 の反応式
[ClH:1].[NH:2]1[CH2:7][CH2:6][CH:5]([O:8][C:9]2[CH:10]=[C:11]3[C:16](=[CH:17][CH:18]=2)[CH:15]=[N:14][CH:13]=[CH:12]3)[CH2:4][CH2:3]1.C(O[C:22]1(O[Si](C)(C)C)[CH2:24][CH2:23]1)C.C([BH3-])#N.[Na+].[OH-].[Na+]>CO.C(O)(=O)C.C(N(CC)CC)C>[ClH:1].[CH:22]1([N:2]2[CH2:7][CH2:6][CH:5]([O:8][C:9]3[CH:10]=[C:11]4[C:16](=[CH:17][CH:18]=3)[CH:15]=[N:14][CH:13]=[CH:12]4)[CH2:4][CH2:3]2)[CH2:24][CH2:23]1

参加物

8

実験手順

300 mg (1.13 mmol) 6-(Piperidine-4-yloxy)-isoquinoline hydrochloride (124) are dissolved in 10 mL of methanol. 202 mg of triethylamine, molecular sieves 4A, 600 mg of glacial acetic acid, 871 mg of (1-Ethoxy-cyclopropyloxy)-trimethyl-silane and 101 mg of sodium cyanoborohydride are added successively and the reaction mixture is heated under reflux for 6 hours. The reaction mixture is cooled to room temperature, 6 mL of 2N sodium hydroxide are added and the reaction mixture is filtered. The filtrate is evaporated, the residue is taken up in dichloromethane, extracted with 2 N sodium hydroxide and brine, dried with sodium sulfate, evaporated to dryness and the crude material is purified by preparative HPLC. The product fractions are evaporated, the product is taken up in 2 N hydrochloric acid and lyophilized.

後処理

  1. temperaturethe reaction mixture is heated
  2. temperatureunder reflux for 6 hours
  3. filtrationthe reaction mixture is filtered
  4. customThe filtrate is evaporated
  5. extractionextracted with 2 N sodium hydroxide and brine
  6. dry with materialdried with sodium sulfate
  7. customevaporated to dryness
  8. customthe crude material is purified by preparative HPLC
  9. customThe product fractions are evaporated

出典と根拠

ORDレコード
ord-494b77e2002b424dae90b060b9ba8090
出典データセット
uspto-grants-2013_08
特許番号
US08501736B2

反応ノート

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