Trifluoroacetic acid → 3-Aminomethyl-5-chloro-4-fluoro-N-methyl-benzamide
Reaction equation
C(OC(=O)[NH:7][CH2:8][C:9]1[CH:14]=[C:13]([C:15](=[O:18])[NH:16][CH3:17])[CH:12]=[C:11]([Cl:19])[C:10]=1[F:20])(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[NH2:7][CH2:8][C:9]1[CH:14]=[C:13]([CH:12]=[C:11]([Cl:19])[C:10]=1[F:20])[C:15]([NH:16][CH3:17])=[O:18]Participants
4
Procedure
was prepared according to Scheme C3 (step B) from (3-chloro-2-fluoro-5-methylcarbamoyl-benzyl)-carbamic acid tert-butyl ester (99 mg, 0.3 mmol) and TFA (0.5 mL) in CH2Cl2. MS (LC-MS): 217.0 [M]+; tR (HPLC conditions c): 2.39 min.
Workup
- customwas prepared
- custom2.39 min.
Sources & evidence
- ORD record
- ord-ad51c25bea264edaa07f8f6ddac7df1d
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09085555B2
Reaction notes
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