Trifluoroacetic acid → HCID 59191501, compound
Reaction equation
C(O)(C(F)(F)F)=O.[CH2:8]([C:15]1[N:20]=[N:19][C:18]([N:21]2[CH2:26][CH2:25][C:24](=O)[CH2:23][CH2:22]2)=[C:17]([CH3:28])[C:16]=1[CH3:29])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[CH2:30]1[C:39]2[C:34](=[CH:35][CH:36]=[CH:37][CH:38]=2)[CH2:33][CH2:32][NH:31]1>>[CH2:8]([C:15]1[N:20]=[N:19][C:18]([N:21]2[CH2:26][CH2:25][CH:24]([N:31]3[CH2:32][CH2:33][C:34]4[C:39](=[CH:38][CH:37]=[CH:36][CH:35]=4)[CH2:30]3)[CH2:23][CH2:22]2)=[C:17]([CH3:28])[C:16]=1[CH3:29])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1Participants
4
Procedure
This compound as a TFA salt is prepared from compound 24 and 1,2,3,4-tetrahydro-isoquinoline following a procedure used in example 56.
Sources & evidence
- ORD record
- ord-32bc8c7a3e154ac683b7056b0dc890cd
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09409871B2
Reaction notes
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