Hydrochloric Acid → HCID 21584389, compound

HRID 369986Notes

Reaction equation

HRID 369986 reaction equation
[CH2:1]1[CH:13]2[N:4]([CH2:5][C:6]3[CH:7]=[CH:8][CH:9]=[CH:10][C:11]=3[CH2:12]2)[CH2:3][CH2:2]1.[N+:14]([O-])([O-:16])=[O:15].[K+].[OH-].[NH4+].[ClH:21]>S(=O)(=O)(O)O.C(O)(C)C.C(O)C>[ClH:21].[N+:14]([C:8]1[CH:9]=[CH:10][C:11]2[CH2:12][CH:13]3[CH2:1][CH2:2][CH2:3][N:4]3[CH2:5][C:6]=2[CH:7]=1)([O-:16])=[O:15]

Participants

8

Procedure

To a solution of 1,2,3,5,10,10a-hexahydropyrrolo[1,2-b]isoquinoline (4.12 g, 23.8 mmol) in concentrated sulfuric acid (100 ml) at -10° C. was added, in portions over 1 h, potassium nitrate (2.40 g, 23.7 mmol). After addition was complete, the reaction mixture was stirred for 1 h before it was poured over ice. The aqueous solution was made basic with concentrated ammonium hydroxide and the product was extracted into dichloromethane (twice). The dried (magnesium sulfate) organic phase was concentrated to give a red oil that solidified on standing. This solid was taken up in isopropanol (100 ml) and hydrogen chloride in ethanol was added until acidic. The solid was collected, washed with isopropanol and dried to give the crude product (3.39 g, 56%). This solid was recrystalized from ethanol to give the title compound (2.16 g, 36%) as an off-white solid, m.p. 231-3° C. (dec.)

Workup

  1. additionAfter addition
  2. additionwas poured over ice
  3. extractionthe product was extracted into dichloromethane (twice)
  4. dry with materialThe dried (magnesium sulfate) organic phase
  5. concentrationwas concentrated
  6. customto give a red oil that
  7. customThe solid was collected
  8. washwashed with isopropanol
  9. customdried
  10. customto give the crude product (3.39 g, 56%)
  11. customThis solid was recrystalized from ethanol

Sources & evidence

ORD record
ord-58de5e365fd742a4ba70a942b4c4f4d1
Source dataset
uspto-grants-2000_10
Patent number
US06140322

Reaction notes

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