Water → HCID 178419968, compound
Reaction equation
C(OC([N:8]1[C@H:13]([C:14]2[NH:15][CH:16]=[C:17]([C:19]3[CH:24]=[CH:23][C:22]([C:25]4[CH:30]=[CH:29][C:28]([C:31]5[N:32]=[C:33]([C@@H:36]6[CH2:44][CH:43]7[CH:38]([CH2:39][CH2:40][CH2:41][CH2:42]7)[N:37]6C(OC(C)(C)C)=O)[NH:34][CH:35]=5)=[CH:27][CH:26]=4)=[CH:21][CH:20]=3)[N:18]=2)[CH:12]2[CH2:52][CH:9]1[CH2:10][CH2:11]2)=O)(C)(C)C.O>CO>[CH:9]12[CH2:52][CH:12]([CH2:11][CH2:10]1)[C@@H:13]([C:14]1[NH:15][CH:16]=[C:17]([C:19]3[CH:20]=[CH:21][C:22]([C:25]4[CH:26]=[CH:27][C:28]([C:31]5[N:32]=[C:33]([C@@H:36]6[CH2:44][CH:43]7[CH:38]([CH2:39][CH2:40][CH2:41][CH2:42]7)[NH:37]6)[NH:34][CH:35]=5)=[CH:29][CH:30]=4)=[CH:23][CH:24]=3)[N:18]=1)[NH:8]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
Compound 8 were taken in 9 ml methanol; 1 ml Conc. HCL and 0.2 ml water was added. Resulting reaction was stirred for 5 h at 50° C. (oil bath temp) completed, after completion of the reaction monitor by HPLC. The resulting slurry was cooled to RT and held with agitation for about 1H. Filtration of the slurry afforded a solid; washed with 15 ml acetone dried directly used in the next reaction.
Workup
- customResulting
- customreaction
- temperatureThe resulting slurry was cooled to RT
- filtrationFiltration of the slurry
- customafforded a solid
- washwashed with 15 ml acetone
- customdried directly
- customused in the next reaction
Sources & evidence
- ORD record
- ord-673eb56f20c2438095516ff5b6b1d4d6
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08835456B1
Reaction notes
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