1,2,3,4-Tetrahydro-1-naphthylamine → HCID 68607966, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH2:9][C@H:10]([NH:14][C:15](=[O:24])OCC2C=CC=CC=2)[C@H:11]2[CH2:13][O:12]2)[CH:5]=[C:6]([F:8])[CH:7]=1.[CH:25]1([NH2:35])[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)CCC1.[CH2:36]([N:39]([CH2:53][CH2:54][CH3:55])[C:40]([C:42]1[CH:43]=[C:44](C=C(CC)C=1)[C:45](O)=[O:46])=[O:41])[CH2:37][CH3:38]>>[CH2:25]([NH:35][CH2:13][C@@H:11]([OH:12])[C@@H:10]([NH:14][C:15]([C:45]1[O:46][C:42]([C:40]([N:39]([CH2:53][CH2:54][CH3:55])[CH2:36][CH2:37][CH3:38])=[O:41])=[CH:43][CH:44]=1)=[O:24])[CH2:9][C:4]1[CH:5]=[C:6]([F:8])[CH:7]=[C:2]([F:1])[CH:3]=1)[C:34]1[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1Participants
4
Procedure
Following the general procedure of EXAMPLEs 4, 5 and 6 and making non-critical variations but using tert-butyl (1S)-2-(3,5-difluorophenyl)-1-[(2S)-oxiranyl]ethylcarbamate (V), H2N—CH2-phenyl (VI) and (CH3—CH2—CH2—)2N—CO—(2,5-furanyl)—CO— (IX), the title compound is obtained, MH+=528.
Sources & evidence
- ORD record
- ord-134abc2b6c2a4027bb38b80b49af9308
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07214715B2
Reaction notes
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