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

HRID 1777091
Notes
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Reaction equation

HRID 1777091 reaction equation
[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
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
80 °C

Procedure

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).

Workup

  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%)

Sources & evidence

ORD record
ord-6e17347667724f0b8bd52c81c4a02248
Source dataset
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09266836B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes