Methanol → HCID 86750572, compound

HRID 2287827Notes

Reaction equation

HRID 2287827 reaction equation
[CH:1]12[NH:18][CH:14]([CH2:15][CH2:16][CH2:17]1)[CH2:13][NH:12][CH2:11][CH2:10][NH:9][CH2:8][CH2:7][NH:6][CH2:5][CH2:4][NH:3][CH2:2]2.CO.[Cl-:21].[Mn+2:22].[Cl-:23]>CCO>[Cl:21][CH:13]1[NH:12][CH2:11][CH2:10][NH:9][CH2:8][CH2:7][NH:6][CH2:5][CH2:4][NH:3][CH2:2][CH:1]2[NH:18][C:14]1([Cl:23])[CH2:15][CH2:16][CH2:17]2.[Mn+2:22]

Participants

5

Procedure

3,6,9,12,18-Pentaazabicyclo[12.3.1]octadecane prepared as in Example 38C (0.405 g, 1.59 mmol) was added to a refluxing solution of anhydrous MeOH (50 ml) containing anhydrous manganese(II) chloride (0.200 g, 1.59 mmo) under a dry nitrogen atmosphere. After refluxing for 2 h, the solution was stirred overnight at room temperature. The solution was taken to dryness. The solid was dissolved in EtOH (10 ml) and the solution was filtered through celite. Ethyl ether was added to the filtrate which induced crystallization of a white solid. The solid was collected by filtration, washed with ethyl ether and dried in vacuo to give 0.43 g (72% yield) of a white solid as product: FAB mass spectrum (NBA) m/z (relative intensity) 380 (M+, 3), 345/347 [(M-Cl)+, 100/2]; Anal. calcd for C14H31N5MnCl2 : C, 40.96; H, 7.67; N, 18.37. Found: C,40.85; H, 7.72; N, 18.32.

Workup

  1. temperatureAfter refluxing for 2 h
  2. filtrationthe solution was filtered through celite
  3. additionEthyl ether was added to the filtrate which
  4. customcrystallization of a white solid
  5. filtrationThe solid was collected by filtration
  6. washwashed with ethyl ether
  7. customdried in vacuo

Sources & evidence

ORD record
ord-da7d7756072d4baa8b929ee062fa2a45
Source dataset
uspto-grants-2000_07
Patent number
US06084093

Reaction notes

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