Water → [(4R,5R)-5-(4-methylsulfonylphenyl)-2-phenyl-4,5-dihydro-1,3-oxazol-4-yl]methanol
Reaction equation
[NH2:1][C@H:2]([CH2:15][OH:16])[C@@H:3]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([CH3:14])(=[O:13])=[O:12])=[CH:7][CH:6]=1)[OH:4].Cl.C(O[C:21]([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)=N)C.C(N(CC)CC)C.O>ClCCCl>[CH3:14][S:11]([C:8]1[CH:7]=[CH:6][C:5]([C@H:3]2[O:4][C:21]([C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[N:1][C@@H:2]2[CH2:15][OH:16])=[CH:10][CH:9]=1)(=[O:13])=[O:12]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
(1R,2R)-2-amino-1-[4-(methylsulfonyl)phenyl]-1,3-propanediol (Compound V wherein R1 is methylsulfonyl) (about 10 g, 0.04077) is reacted at about 0° C. in a reaction vessel with benzenecarboximidic acid ethyl ester hydrochloride (Compound IV hydrochloride wherein R2 is phenyl and R4 is ethyl) (about 8.3 g, 0.0448 moles) in 1,2-dichloroethane (about 650 mL) containing triethylamine (about 4.1 g, 0.04077 moles). Next, water (about 500 mL) is added. The resulting solids are filtered, then dried to yield (4R,5R)-4,5-Dihydro-5-[4-(methylsulfonyl)phenyl]-2-phenyl-4-oxazolemethanol (Compound II wherein R1 is methylsulfonyl and R2 is phenyl).
Workup
- filtrationThe resulting solids are filtered
- customdried
Sources & evidence
- ORD record
- ord-445ee076caeb4c45bd35ce7d588dff06
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08314252B2
Reaction notes
Loading…