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Hydrochloric Acid → HCID 21928083, 화합물

HRID 1243783
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HRID 1243783 반응식
C(OC(=O)[NH:7][CH2:8][CH:9]([C:11]1[CH:16]=[CH:15][C:14]([C:17](=[O:26])[NH:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[CH:13][N:12]=1)[OH:10])(C)(C)C.[ClH:28].O1CCOCC1>CCOC(C)=O>[ClH:28].[ClH:28].[NH2:7][CH2:8][CH:9]([C:11]1[CH:16]=[CH:15][C:14]([C:17]([NH:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[O:26])=[CH:13][N:12]=1)[OH:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 312751,4-DioxaneHCID 21064723HCID 21064723, 화합물

생성물 1

HCID 21928083HCID 21928083, 화합물

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

[2-(5-Benzylcarbamoyl-pyridin-2-yl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester (47.0 mg, 0.129 mmol) was dissolved into 2 mL of EtOAc and 4.0 N HCl in dioxane (1.0 mL, 4 mmol) was added. The reaction was allowed to stir overnight. The resulting precipitate was triturated with 3×5 mL of THF and concentrated on a rotary evaporator to dryness to give 43 mg of 6-(2-amino-1-hydroxy-ethyl)-N-benzyl-nicotinamide 2HCl.

후처리

  1. additionwas added
  2. customThe resulting precipitate was triturated with 3×5 mL of THF
  3. concentrationconcentrated on a rotary evaporator to dryness

출처 및 근거

ORD 기록
ord-cc0c0361f72d47efb02a5a761b907d74
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07119102B2

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