Hydrochloric Acid → HCID 86752687, compound

HRID 1737917Notes

Reaction equation

HRID 1737917 reaction equation
[C:1]([O:5][C:6]([C:8]1[N:9](C(OC(C)(C)C)=O)[C:10]2[C:15]([C:16]=1[CH:17]([CH:19]1[C:23](=[O:24])[N:22]([C:25](OC(C)(C)C)=O)N(C3C4CC5CC(CC3C5)C4)[CH2:20]1)O)=[C:14]([Cl:42])[CH:13]=[C:12]([Cl:43])[CH:11]=2)=[O:7])(C)(C)C.Cl>C(O)C>[Cl:42][C:14]1[CH:13]=[C:12]([Cl:43])[CH:11]=[C:10]2[C:15]=1[C:16](/[CH:17]=[C:19]1/[C:23](=[O:24])[N:22]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH2:25][CH2:20]/1)=[C:8]([C:6]([O:5][CH3:1])=[O:7])[NH:9]2

Participants

4

Procedure

Intermediate 4 (700 mg) was suspended in ethanol (95%) (10 ml), hydrochloric acid (10 ml, 6M) was added and the heterogeneous mixture refluxed for 10 h. The suspension was cooled to room temperature and the solid filtered, washed with further portions of 6M hydrochloric acid and finally vacuum dried to yield the title compound (427 mg,) as a white solid.

Workup

  1. temperaturethe heterogeneous mixture refluxed for 10 h
  2. filtrationthe solid filtered
  3. washwashed with further portions of 6M hydrochloric acid and finally vacuum
  4. customdried

Sources & evidence

ORD record
ord-6e2a38c877ea45768d3d0735c40d22b7
Source dataset
uspto-grants-1999_10
Patent number
US05962496

Reaction notes

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