Trifluoroacetic acid → (3-Aminomethyl-5-chloro-4-fluoro-phenyl)-morpholin-4-yl-methanone
Reaction equation
C(OC(=O)[NH:7][CH2:8][C:9]1[CH:14]=[C:13]([C:15]([N:17]2[CH2:22][CH2:21][O:20][CH2:19][CH2:18]2)=[O:16])[CH:12]=[C:11]([Cl:23])[C:10]=1[F:24])(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[NH2:7][CH2:8][C:9]1[CH:14]=[C:13]([C:15]([N:17]2[CH2:22][CH2:21][O:20][CH2:19][CH2:18]2)=[O:16])[CH:12]=[C:11]([Cl:23])[C:10]=1[F:24]Participants
4
Procedure
was prepared according to Scheme C3 (step B) from [3-chloro-2-fluoro-5-(morpholine-4-carbonyl)-benzyl]-carbamic acid tert-butyl ester (72 mg, 0.19 mmol) and TFA (1 mL) in CH2Cl2. MS (LC-MS): 273.0 [M]+; tR (HPLC conditions c): 2.64 min.
Workup
- customwas prepared
- custom2.64 min.
Sources & evidence
- ORD record
- ord-5b9695d8875a4ecb9022e712ae575014
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09085555B2
Reaction notes
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