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Sodium borohydride → 6-(1-Hydroxyethyl)pyrrolo[1,2-a]pyrazine

HRID 233462
Notes
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Reaction equation

HRID 233462 reaction equation
[C:1]([C:4]1[N:8]2[CH:9]=[CH:10][N:11]=[CH:12][C:7]2=[CH:6][CH:5]=1)(=[O:3])[CH3:2].[BH4-].[Na+]>O>[OH:3][CH:1]([C:4]1[N:8]2[CH:9]=[CH:10][N:11]=[CH:12][C:7]2=[CH:6][CH:5]=1)[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 4311764Sodium borohydrideHCID 233564476-Acetylpyrrolo[1,2-a]pyrazine

Product 1

HCID 233564716-(1-Hydroxyethyl)pyrrolo[1,2-a]pyrazineYield 69.1%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

2.0 g of 6-acetylpyrrolo[1,2-a]pyrazine prepared in Preparation Example 15 was added to 30 ml of water; and 0.5 g of sodium borohydride was added thereto. After reacting at 50° C. for 2 hours, the mixture was extracted with ethyl acetate (50 ml×3). The residue was chromatographed over silica gel to yield 1.4 g of 6-(1-hydroxyethyl)pyrrolo[1,2-a]pyrazine.

Workup

  1. extractionthe mixture was extracted with ethyl acetate (50 ml×3)
  2. customThe residue was chromatographed over silica gel

Sources & evidence

ORD record
ord-4c9c57ef765b4926a45c20f34eea9f9f
Source dataset
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05593984

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes