Boron Trichloride → HCID 59608296, compound
Reaction equation
C([O:8][C:9](=[O:39])[C@H:10]([CH3:38])[CH2:11][C@H:12]([NH:26][C:27]([C:29]1[O:30][CH:31]=[C:32]([O:36][CH3:37])[C:33](=[O:35])[CH:34]=1)=[O:28])[CH2:13][C:14]1[CH:19]=[CH:18][C:17]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[CH:16][CH:15]=1)C1C=CC=CC=1.B(Cl)(Cl)Cl>C(Cl)Cl>[C:17]1([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH:18]=[CH:19][C:14]([CH2:13][C@@H:12]([NH:26][C:27]([C:29]2[O:30][CH:31]=[C:32]([O:36][CH3:37])[C:33](=[O:35])[CH:34]=2)=[O:28])[CH2:11][C@@H:10]([CH3:38])[C:9]([OH:39])=[O:8])=[CH:15][CH:16]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Next, To a solution of (2R,4S)-5-biphenyl-4-yl-4-[(5-methoxy-4-oxo-4H-pyran-2-carbonyl)-amino]-2-methyl-pentanoic acid benzyl ester in methylene chloride (1 mL) is added BCl3 (0.12 mL of a 1M solution in methylene chloride) and the mixture is stirred at room temperature for 18 hours. An additional 0.12 mL of the BCl3 solution is added and stirring is continued for 5 hours. An additional 0.12 mL of the BCl3 solution is added and stirring is continued for 18 hours. The mixture is quenched with water (2 drops) and DMF (1 mL) is added. The solution is purified by preparative HPLC using a gradient of 10% MeCN/water to 100% MeCN (0.1% TFA) to elute the title compound; HPLC Retention time 1.28 minutes (condition C): MS 436.1 (M+1)
Workup
- stirringstirring
- waitis continued for 5 hours
- stirringstirring
- waitis continued for 18 hours
- customThe mixture is quenched with water (2 drops) and DMF (1 mL)
- additionis added
- customThe solution is purified by preparative HPLC
- washto elute the title compound
Sources & evidence
- ORD record
- ord-584eaeba929e40618f84c6740b14bfcc
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263629B2
Reaction notes
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