Dichloromethane → HCID 58700790, compound
Reaction equation
C([O:8][C:9]1[CH:14]=[CH:13][C:12]([N:15]2[C:19]([CH:20]3[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]3)=[CH:18][C:17](/[CH:26]=[C:27](\[CH3:33])/[C:28]([O:30][CH2:31][CH3:32])=[O:29])=[N:16]2)=[CH:11][CH:10]=1)C1C=CC=CC=1.B(Cl)(Cl)Cl.ClCCl>>[CH:20]1([C:19]2[N:15]([C:12]3[CH:11]=[CH:10][C:9]([OH:8])=[CH:14][CH:13]=3)[N:16]=[C:17](/[CH:26]=[C:27](\[CH3:33])/[C:28]([O:30][CH2:31][CH3:32])=[O:29])[CH:18]=2)[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25]1Participants
4
Procedure
According to the procedure for preparation of 4.3, debenzylation of 10.1 (440 mg, 0.99 mmol) with 1M BCl3 in dichloromethane (4.95 ml, 4.95 mmol) yielded 353 mg (100%) of 10.3. MS (ESI) 355.4 (MH+).
Sources & evidence
- ORD record
- ord-076d7981c8504120ba307af9c55fe8e0
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07112601B2
Reaction notes
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