Oxalic Acid → HCID 19045416, compound

HRID 1591163Notes

Reaction equation

HRID 1591163 reaction equation
[NH:1]1[CH2:6][CH2:5][CH2:4][C:3]2([CH2:11][C:10](=[O:12])[C:9]3[CH:13]=[CH:14][CH:15]=[CH:16][C:8]=3[O:7]2)[CH2:2]1.S(O[CH2:22][CH2:23][C:24]1[CH:29]=[CH:28][C:27]([NH:30][S:31]([CH3:34])(=[O:33])=[O:32])=[CH:26][CH:25]=1)(=O)(=O)C.C(=O)(O)[O-].[Na+].[C:40]([OH:45])(=[O:44])[C:41]([OH:43])=[O:42]>C(O)C>[C:40]([OH:45])(=[O:44])[C:41]([OH:43])=[O:42].[CH3:34][S:31]([NH:30][C:27]1[CH:28]=[CH:29][C:24]([CH2:23][CH2:22][N:1]2[CH2:6][CH2:5][CH2:4][C:3]3([CH2:11][C:10](=[O:12])[C:9]4[CH:13]=[CH:14][CH:15]=[CH:16][C:8]=4[O:7]3)[CH2:2]2)=[CH:25][CH:26]=1)(=[O:33])=[O:32]

Participants

6

Procedure

A solution of 560 mg (258 mmole) of 3,4-dihydrospiro-[(2H)-1-benzopyran-2,3'-piperidine]4-one in 20 mL ethanol was treated with 880 mg (3 mmoles) of 2-(4-methanesulfonamidophenyl)ethyl mesylate and 0.5 g sodium bicarbonate and heated to reflux for 48 hours. The reaction was cooled to room temperature, poured into saturated sodium bicarbonate and extracted with ethyl acetate. The ethyl acetate solution was dried over magnesium sulfate, filtered and concentrated in vacuo. The crude material was treated with 1 eq. oxalic acid and the salt was recrystallized from acetone to give product with mp=204°-210° C.

Workup

  1. temperatureheated
  2. temperatureto reflux for 48 hours
  3. extractionextracted with ethyl acetate
  4. dry with materialThe ethyl acetate solution was dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customthe salt was recrystallized from acetone
  8. customto give product with mp=204°-210° C.

Sources & evidence

ORD record
ord-dcd5c921033d4715be6c1a437f41c168
Source dataset
uspto-grants-1993_04
Patent number
US05206240

Reaction notes

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