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Hydrochloric Acid → 2-(Cyclobutylcarbonyl)-N-hydroxy-1,2,3,4-tetrahydroisoquinoline-6-carboxamide

HRID 2036857
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반응식

HRID 2036857 반응식
[CH:1]1([C:5]([N:7]2[CH2:16][CH2:15][C:14]3[C:9](=[CH:10][CH:11]=[C:12]([C:17]([NH:19][O:20]C4CCCCO4)=[O:18])[CH:13]=3)[CH2:8]2)=[O:6])[CH2:4][CH2:3][CH2:2]1.Cl>O.CO>[CH:1]1([C:5]([N:7]2[CH2:16][CH2:15][C:14]3[C:9](=[CH:10][CH:11]=[C:12]([C:17]([NH:19][OH:20])=[O:18])[CH:13]=3)[CH2:8]2)=[O:6])[CH2:2][CH2:3][CH2:4]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 866565922-(cyclobutylcarbonyl)-N-(tetrahydro-2H-pyran-2-yloxy)-1,2,3,4-tetrahydroisoquinoline-6-carboxamide

생성물 1

HCID 442303902-(Cyclobutylcarbonyl)-N-hydroxy-1,2,3,4-tetrahydroisoquinoline-6-carboxamide

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

160 mg of 2-(cyclobutylcarbonyl)-N-(tetrahydro-2H-pyran-2-yloxy)-1,2,3,4-tetrahydroisoquinoline-6-carboxamide and 2 ml of a 0.1M solution of HCl in water in 2 ml methanol are stirred overnight at ambient temperature. The reaction mixture is evaporated and the residue is treated with acetonitrile. 53 mg of nearly colorless crystals are obtained. MH+=275.1

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후처리

  1. customThe reaction mixture is evaporated
  2. additionthe residue is treated with acetonitrile
  3. custom53 mg of nearly colorless crystals are obtained

출처 및 근거

ORD 기록
ord-ecee488d377c4878a3ac5053e5573711
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08575193B2

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