Hydrochloride methanol → 4-(4-Ethyl-5-isoquinolyl)aminopiperidine hydrochloride

HRID 10541ノート

反応式

HRID 10541 の反応式
[CH2:1]([C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][C:11]=2[NH:13][CH:14]2[CH2:19][CH2:18][N:17](C(OC(C)(C)C)=O)[CH2:16][CH2:15]2)[CH:6]=[N:5][CH:4]=1)[CH3:2].[ClH:27].CO>>[ClH:27].[CH2:1]([C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][C:11]=2[NH:13][CH:14]2[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]2)[CH:6]=[N:5][CH:4]=1)[CH3:2]

参加物

3

反応物 2

HCID 21893726Hydrochloride methanolHCID 219798934-(4-Ethyl-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine

生成物 1

HCID 219797434-(4-Ethyl-5-isoquinolyl)aminopiperidine hydrochloride

実験手順

According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 82 (93.7 mg) and 10% hydrogen chloride/methanol solution (2 ml). The reaction mixture was cooled to room temperature, and then the solvent was evaporated under reduced pressure. The residue was added with methanol (1 ml) and diethyl ether (3 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (63.2 mg) as light yellow powdery solid.

後処理

  1. custom(50° C., 2 hours)
  2. customthe solvent was evaporated under reduced pressure
  3. additionThe residue was added with methanol (1 ml) and diethyl ether (3 ml)
  4. customThe deposited precipitates
  5. filtrationwere collected by filtration
  6. washwashed with diethyl ether

出典と根拠

ORDレコード
ord-749ac926d34d4575ae04f26fcd6095f9
出典データセット
uspto-grants-2006_08
特許番号
US07094789B2

反応ノート

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