Hydrochloric Acid → Erlotinib Hydrochloride

HRID 2092907Notes

Reaction equation

HRID 2092907 reaction equation
[CH3:1][O:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[C:8]2[C:20]([NH:21][C:22]3[CH:23]=[CH:24][CH:25]=[C:26]([C:28]#[CH:29])[CH:27]=3)=[N:19][CH:18]=[N:17][C:9]2=[CH:10][C:11]=1[O:12][CH2:13][CH2:14][O:15][CH3:16].FC(F)(F)C([O-])=O.[ClH:37]>O>[CH3:1][O:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[C:8]2[C:20]([NH:21][C:22]3[CH:23]=[CH:24][CH:25]=[C:26]([C:28]#[CH:29])[CH:27]=3)=[N:19][CH:18]=[N:17][C:9]2=[CH:10][C:11]=1[O:12][CH2:13][CH2:14][O:15][CH3:16].[ClH:37]

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 86664461HCID 86664461, compound

Product 1

HCID 176871Erlotinib Hydrochloride

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

Erlotinib trifluoroacetate salt (10 g) was charged into deionized water (DI water) (80 ml) at 25° C. to 30° C. 35% Concentrated hydrochloric acid (aqueous, 12 ml) was added slowly to reaction mixture at 25° C. to 30° C. and stirred for about 2 hours at 25° C. to 30° C. The solid obtained was filtered, washed with DI water (2×15 ml) and dried under vacuum for about 18 hours at 40° C. to 45° C. to give erlotinib hydrochloride.

Workup

  1. customThe solid obtained
  2. filtrationwas filtered
  3. washwashed with DI water (2×15 ml)
  4. customdried under vacuum for about 18 hours at 40° C. to 45° C.

Sources & evidence

ORD record
ord-de52347d2fc1435b8bca86e55fe2767a
Source dataset
uspto-grants-2013_05
Patent number
US08440823B2

Reaction notes

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