Lithium Hydroxide → HCID 131729425、化合物

HRID 425396ノート

反応式

HRID 425396 の反応式
[OH-].[Li+].[C:3]([NH:6][CH:7]([CH2:12][C:13]1[CH:18]=[CH:17][C:16]([C:19]2[C:20]([NH:25][C:26]([O:28][C:29]([CH3:32])([CH3:31])[CH3:30])=[O:27])=[N:21][N:22]([CH3:24])[CH:23]=2)=[CH:15][CH:14]=1)[C:8](OC)=[O:9])(=[O:5])[CH3:4].C(=O)(O)[O-].[Na+].[NH2:38][CH2:39][CH:40]([OH:47])[CH2:41][C:42]([CH3:46])([CH3:45])[CH2:43][CH3:44].Cl.CN(C)CCCN=C=NCC.ON1C2C=CC=CC=2N=N1>O1CCCC1.O.O.C(Cl)Cl>[C:29]([O:28][C:26](=[O:27])[NH:25][C:20]1[C:19]([C:16]2[CH:17]=[CH:18][C:13]([CH2:12][CH:7]([NH:6][C:3](=[O:5])[CH3:4])[C:8]([NH:38][CH2:39][CH:40]([OH:47])[CH2:41][C:42]([CH3:46])([CH3:45])[CH2:43][CH3:44])=[O:9])=[CH:14][CH:15]=2)=[CH:23][N:22]([CH3:24])[N:21]=1)([CH3:31])([CH3:30])[CH3:32]

参加物

10

反応物 6

HCID 3939Lithium HydroxideHCID 757711-HydroxybenzotriazoleHCID 516892Sodium BicarbonateHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 55289824HCID 55289824、化合物HCID 66705663methyl 2-(acetylamino)-3-(4-{3-[(tert-butoxycarbonyl)amino]-1-methyl-1H-pyrazol-4-yl}phenyl)propanoate

生成物 1

HCID 131729425HCID 131729425、化合物

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 6344Dichloromethane溶媒HCID 21881883Oxolane--water (1/1)溶媒

実験手順

Lithium hydroxide (444 mg, 10.8 mmol) was added to an ambient temperature solution of methyl 2-(acetylamino)-3-(4-{3-[(tert-butoxycarbonyl)amino]-1-methyl-1H-pyrazo 1-4-yl}phenyl)propanoate (450 mg, 1.08 mmol) in tetrahydrofuran/water (10:1) (11 mL). After stirring at ambient temperature for 1 h, the reaction mixture was diluted with water and extracted with ethyl acetate. The aqueous phase was acidified with 1.5 N hydrochloric acid and extracted with ethyl acetate. The combined organic extracts were dried (magnesium sulfate) and concentrated in vacuo. Sodium bicarbonate (727 mg, 8.66 mmol) was added to an ambient temperature solution of the crude residue, 1-amino-4,4-dimethylhexan-2-ol (314 mg, 2.16 mmol), 1-[3-(dimethylamino) propyl]-3-ethylcarbodiimide hydrochloride (415 mg, 2.16 mmol) and 1-hydroxybenzotriazole (292 mg, 2.16 mmol) in methylene chloride (20 mL). After stirring at ambient temperature overnight, the reaction was quenched with water and extracted with methylene chloride and ethyl acetate. The combined organic extracts were dried (magnesium sulfate) and concentrated in vacuo. Chromatography over silica eluting with 0-100% ethyl acetate/hexane afforded tert-butyl[4-(4-{2-(acetylamino)-3-[(2-hydroxy-4,4-dimethylhexyl)amino]-3-oxopropyl}phenyl)-1-methyl-1H-pyrazol-3-yl]carbamate.

後処理

  1. extractionextracted with ethyl acetate
  2. extractionextracted with ethyl acetate
  3. dry with materialThe combined organic extracts were dried (magnesium sulfate)
  4. concentrationconcentrated in vacuo
  5. stirringAfter stirring at ambient temperature overnight
  6. customthe reaction was quenched with water
  7. extractionextracted with methylene chloride and ethyl acetate
  8. dry with materialThe combined organic extracts were dried (magnesium sulfate)
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-5d6538de3d7a408980d87525ea0b714b
出典データセット
uspto-grants-2012_01
特許番号
US08106070B2

反応ノート

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