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Methanol → HCID 68912341, compound

HRID 2102602
Notes
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Reaction equation

HRID 2102602 reaction equation
I[CH2:2][CH:3]([CH3:17])[CH2:4][N:5]1[C:10]2[CH:11]=[C:12](C)[CH:13]=[CH:14][C:9]=2[O:8][CH2:7][C:6]1=[O:16].CC[N:20]([CH2:23][CH3:24])[CH2:21][CH3:22].[CH3:25][OH:26]>>[CH3:25][O:26][C:12]1[CH:13]=[CH:14][C:9]2[O:8][CH2:7][C:6](=[O:16])[N:5]([CH2:4][C@H:3]([CH3:17])[CH2:2][N:20]3[CH2:21][CH2:22][CH:7]([O:8][CH2:9][CH2:10][CH3:11])[CH2:24][CH2:23]3)[C:10]=2[CH:11]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 887MethanolHCID 8471TriethylamineHCID 689085494-(3-iodo-2-methylpropyl)-6-methyl-4H-benzo[1,4]oxazin-3-one

Product 1

HCID 68912341HCID 68912341, compound

Conditions

Temperature
60 °C

Procedure

A 7 mL vial was charged with the crude 4-(3-iodo-2-methylpropyl)-6-methyl-4H-benzo[1,4]oxazin-3-one (1 equiv), Et3N (0.5 mL) and the secondary amine (1.2-1.5 equiv). This mixture was shaken at 60° C. for 72 h and thereafter diluted with MeOH (10 mL) and concentrated with basic Al2O3 (2 g) and purified by flash chromatography.

Workup

  1. concentrationconcentrated with basic Al2O3 (2 g)
  2. custompurified by flash chromatography

Sources & evidence

ORD record
ord-cd3ee61d40914144852c72a83fbb0c88
Source dataset
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07576078B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes