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Ammonia → (2R)-1-amino-3-(1,2,3,4-tetrahydroisoquinolin-2-yl)propan-2-ol

HRID 1429422
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HRID 1429422 반응식
[O:1]1[CH2:3][C@@H:2]1[CH2:4][N:5]1[CH2:14][CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6]1.[NH3:15]>CCO>[NH2:15][CH2:3][C@@H:2]([OH:1])[CH2:4][N:5]1[CH2:14][CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6]1
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참가 물질

4

반응물 2

HCID 222AmmoniaHCID 30076572(S)-2-(oxiran-2-ylmethyl)-1,2,3,4-tetrahydroisoquinoline

생성물 1

HCID 25312351(2R)-1-amino-3-(1,2,3,4-tetrahydroisoquinolin-2-yl)propan-2-ol수율 90%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
80 °C

실험 절차

To a solution of (S)-2-(oxiran-2-ylmethyl)-1,2,3,4-tetrahydroisoquinoline (2.2 g, 0.012 mol) in EtOH (30 mL), NH3 was bubbled to the solution under −78° C. The reaction mixture was then sealed and heated at 80° C. for 3 h. After LCMS indicated completion of the reaction, the mixture was concentrated and the crude product was used in next step without further purification (2.2 g, Yield 90%). LCMS (m/z): 207.1 (M+1).

후처리

  1. customThe reaction mixture was then sealed
  2. customcompletion of the reaction
  3. concentrationthe mixture was concentrated
  4. customthe crude product was used in next step without further purification (2.2 g, Yield 90%)

출처 및 근거

ORD 기록
ord-54d34772943f4b9e9896b7754a60e6b6
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08940726B2

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