Hydrochloric Acid → HCID 20819619, compound

HRID 583752Notes

Reaction equation

HRID 583752 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH:9][C:10]2[C:19]3[C:14](=[CH:15][C:16]([O:33][CH3:34])=[C:17]([O:20][C@H:21]4[CH2:25][CH2:24][N:23](C(OC(C)(C)C)=O)[CH2:22]4)[CH:18]=3)[N:13]=[CH:12][N:11]=2)[CH:5]=[CH:6][C:7]=1[F:8].[ClH:35]>O1CCOCC1>[ClH:1].[ClH:35].[Cl:1][C:2]1[CH:3]=[C:4]([NH:9][C:10]2[C:19]3[C:14](=[CH:15][C:16]([O:33][CH3:34])=[C:17]([O:20][C@H:21]4[CH2:25][CH2:24][NH:23][CH2:22]4)[CH:18]=3)[N:13]=[CH:12][N:11]=2)[CH:5]=[CH:6][C:7]=1[F:8]

Participants

4

Procedure

A solution of 370 mg 4-[(3-chloro-4-fluoro-phenyl)amino]-6-[(S)-1-(tert.-butyloxy-carbonyl)-pyrrolidin-3-yloxy]-7-methoxy-quinazoline in 5 ml dioxane is combined with 0.32 ml concentrated hydrochloric acid and stirred overnight at ambient temperature. The precipitate formed is suction filtered and washed with copious amounts of dioxane. The crude product is dissolved in a little methanol and re-precipitated by the addition of the same amount of ethyl acetate. The white solid thus obtained is suction filtered and dried.

Workup

  1. customThe precipitate formed
  2. filtrationfiltered
  3. washwashed with copious amounts of dioxane
  4. dissolutionThe crude product is dissolved in a little methanol
  5. customre-precipitated by the addition of the same amount of ethyl acetate
  6. customThe white solid thus obtained
  7. filtrationis suction filtered
  8. customdried

Sources & evidence

ORD record
ord-aeb2ba54710b4be18325d8b34d783e3c
Source dataset
uspto-grants-2005_08
Patent number
US06924285B2

Reaction notes

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