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Dimethylamine → HCID 13726415, compound

HRID 4867
Notes
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Reaction equation

HRID 4867 reaction equation
[CH3:1][NH:2][CH3:3].Cl[CH2:5][CH2:6][CH:7]1[CH2:13][N:12]([CH3:14])[C:11](=[S:15])[C:10]2[CH:16]=[C:17]([N+:20]([O-:22])=[O:21])[CH:18]=[CH:19][C:9]=2[O:8]1>>[CH3:1][N:2]([CH3:3])[CH2:5][CH2:6][CH:7]1[CH2:13][N:12]([CH3:14])[C:11](=[S:15])[C:10]2[CH:16]=[C:17]([N+:20]([O-:22])=[O:21])[CH:18]=[CH:19][C:9]=2[O:8]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 674DimethylamineHCID 13726304HCID 13726304, compound

Product 1

HCID 13726415HCID 13726415, compound

Procedure

To 50 ml of freshly collected dimethylamine was added 4.25 g (0.014 mole) of 2-(2-chloroethyl)-2,3-dihydro-4-methyl-7-nitro-1,4-benzoxazepine-5(4H)-thione. The reaction flask was sealed tightly and allowed to stand at room temperature for 6 days. The dimethylamine was evaporated at room temperature. The solid residue was taken up in methylene chloride, washed twice with 1N hydroxide and once with water, dried over sodium sulfate, filtered and concentrated by rotary evaporation. Approximately 0.8 g of the crude solid residue was triturated with isopropyl/ether to give the crystalline free base, m.p. 104°-109° C.

Workup

  1. customThe reaction flask was sealed tightly
  2. customThe dimethylamine was evaporated at room temperature
  3. washwashed twice with 1N hydroxide and once with water
  • dry with materialdried over sodium sulfate
  • filtrationfiltered
  • concentrationconcentrated by rotary evaporation
  • customApproximately 0.8 g of the crude solid residue was triturated with isopropyl/ether
  • customto give the crystalline free base, m.p. 104°-109° C.
  • Sources & evidence

    ORD record
    ord-f1df6ffd3002451e8e3a249fd7ae56eb
    Source dataset
    uspto-grants-1988_02
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04727152

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes