Morpholine → HCID 13726355, compound

HRID 1194246Notes

Reaction equation

HRID 1194246 reaction equation
Cl[CH2:2][CH2:3][CH:4]1[CH2:10][N:9]([CH2:11][CH3:12])[C:8](=[O:13])[C:7]2[CH:14]=[CH:15][CH:16]=[CH:17][C:6]=2[N:5]1[CH3:18].[NH:19]1[CH2:24][CH2:23][O:22][CH2:21][CH2:20]1>>[CH2:11]([N:9]1[C:8](=[O:13])[C:7]2[CH:14]=[CH:15][CH:16]=[CH:17][C:6]=2[N:5]([CH3:18])[CH:4]([CH2:3][CH2:2][N:19]2[CH2:24][CH2:23][O:22][CH2:21][CH2:20]2)[CH2:10]1)[CH3:12]

Participants

3

Reactant 2

HCID 8083MorpholineHCID 13726307HCID 13726307, compound

Product 1

HCID 13726355HCID 13726355, compoundYield 61%

Procedure

A solution of 30 g (0.112 mole) of 2-(2-chloroethyl)-4-ethyl-1-methyl-1,2,3,4-tetrahydro-5H-1,4-benzodiazepin-5-one in 70 ml of morpholine was refluxed for 3 hrs, concentrated on the rotary evaporator and the residue partitioned between chloroform and dilute sodium hydroxide. The chloroform was dried over anhydrous sodium sulfate and concentrated on the rotary evaporator. The residue was crystallized twice from isopropyl ether containing a small amount of ethanol, m.p. 128°-148° C. Recrystallization from toluene gave 19.5 g (61%) of product, m.p. 128°-148° C.

Workup

  1. concentrationconcentrated on the rotary evaporator
  2. customthe residue partitioned between chloroform and dilute sodium hydroxide
  3. dry with materialThe chloroform was dried over anhydrous sodium sulfate
  4. concentrationconcentrated on the rotary evaporator
  5. customThe residue was crystallized twice from isopropyl ether containing a small amount of ethanol, m.p. 128°-148° C
  6. customRecrystallization from toluene

Sources & evidence

ORD record
ord-ab6f34b9054a4aa8b5a3a78267bd58ad
Source dataset
uspto-grants-1989_03
Patent number
US04812565

Reaction notes

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