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Butylamine → HCID 31094, compound

HRID 863220
Notes
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Reaction equation

HRID 863220 reaction equation
C(O[C:4]([CH:6]1[CH2:11][NH:10][C:9]2[CH:12]=[CH:13][CH:14]=[CH:15][C:8]=2[O:7]1)=[O:5])C.[CH2:16]([NH2:20])[CH2:17][CH2:18][CH3:19]>>[CH2:16]([NH:20][C:4]([CH:6]1[CH2:11][NH:10][C:9]2[CH:12]=[CH:13][CH:14]=[CH:15][C:8]=2[O:7]1)=[O:5])[CH2:17][CH2:18][CH3:19]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 8007ButylamineHCID 31090Ethyl 3,4-dihydro-2H-1,4-benzoxazine-2-carboxylate

Product 1

HCID 31094HCID 31094, compound

Conditions

Temperature
60 °C

Procedure

A mixture of 600 mg of 2(R,S)-ethoxycarbonyl-3,4-dihydro-2H-1,4-benzoxazine (Example 16)) and 1.2 ml of butylamine is stirred at 60° C. for 1 h. The reaction mixture is concentrated and the residue is purified directly by means of FC over 50 g of silica gel with a 20:1 mixture of methylene chloride and diethyl ether as the mobile phase. 2(R,S)-Butylaminocarbonyl-3,4-dihydro-2H-1,4-benzoxazine is obtained: Rf (20:1-mixture of methylene chloride and diethyl ether)=0.32.

Workup

  1. concentrationThe reaction mixture is concentrated
  • customthe residue is purified directly by means of FC over 50 g of silica gel with a 20:1 mixture of methylene chloride and diethyl ether as the mobile phase
  • Sources & evidence

    ORD record
    ord-b38edd0aab304f57b3138438e2f9bf81
    Source dataset
    uspto-grants-1998_02
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05719141

    Reaction notes

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    On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes