Hydrochloric Acid → HCID 20819619, compound

HRID 1798731Notes

Reaction equation

HRID 1798731 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-5d83adaa38df4e4f802d1ac968ffcea8
Source dataset
uspto-grants-2013_01
Patent number
US08343982B2

Reaction notes

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