Hydrochloric Acid → HCID 13823460, compound

HRID 2226849Notes

Reaction equation

HRID 2226849 reaction equation
Br[CH2:2][CH2:3][CH2:4][CH2:5][C:6]1[C:7](=[O:23])[N:8]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:9]2[C:14]([C:15]=1[OH:16])=[CH:13][CH:12]=[CH:11][N:10]=2.C(N(CC)CC)C.O.Cl>C(Cl)Cl>[C:17]1([N:8]2[C:9]3[C:14](=[CH:13][CH:12]=[CH:11][N:10]=3)[C:15](=[O:16])[C:6]3([CH2:5][CH2:4][CH2:3][CH2:2]3)[C:7]2=[O:23])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

6

Procedure

A suspension of 3-(4-bromobutyl)-4-hydroxy-1-Phenyl-1,8-naphthyridin-2(1H)one (5g.) in methylene chloride (350 ml.), in an atmosphere of nitrogen, was stirred at room temperature and to it was added triethylamine (4.1 ml.). The mixture was stirred at room temperature for 16 hrs. Water (300 ml.) was added and the aqueous layer was adjusted to pH 4.5 with hydrochloric acid. The organic layer was separated and the aqueous layer was back-extracted with methylene chloride. The combined organic layers were washed with water, dried (Na2SO4) , filtered and evaporated to yield a solid which was recrystallized from-isopropanol to yield 1'-phenylspiro[cyclopentane-1,3'-(1,8) naphthyridine]2',4'-(1'H)dione, m.p. 178°-179° C.

Workup

  1. stirringThe mixture was stirred at room temperature for 16 hrs
  2. customThe organic layer was separated
  3. extractionthe aqueous layer was back-extracted with methylene chloride
  4. washThe combined organic layers were washed with water
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. customevaporated
  8. customto yield a solid which
  9. customwas recrystallized from-isopropanol

Sources & evidence

ORD record
ord-47d3892c4ad9478dab7a9caeb71fb7c7
Source dataset
uspto-grants-1994_09
Patent number
US05350755

Reaction notes

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