N-Ethylbenzylamine → HCID 22504801, compound
Reaction equation
COC(=O)COC1C=C(OC)C(SCCC=O)=CC=1C.C(NCC)C1C=CC=CC=1.C[O:32][C:33](=[O:64])[CH2:34][O:35][C:36]1[CH:41]=[C:40]([O:42][CH3:43])[C:39]([S:44][CH2:45][CH2:46][CH2:47][N:48]([CH2:61][CH3:62])[C:49]2[CH:54]=[CH:53][C:52]([C:55]3[CH:60]=[CH:59]C=CC=3)=CN=2)=[CH:38][C:37]=1[CH3:63]>>[CH2:49]([N:48]([CH2:61][CH3:62])[CH2:47][CH2:46][CH2:45][S:44][C:39]1[C:40]([O:42][CH3:43])=[CH:41][C:36]([O:35][CH2:34][C:33]([OH:32])=[O:64])=[C:37]([CH3:63])[CH:38]=1)[C:54]1[CH:53]=[CH:52][CH:55]=[CH:60][CH:59]=1Participants
4
Procedure
Compound 64A and benzyl-ethyl-amine were reacted in a manner analogous to Compound 64C to give the title product. MS m/z 418 (M+1).
Sources & evidence
- ORD record
- ord-fa297b84455745099ec093ffbe4e550b
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07244763B2
Reaction notes
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