(R)-1,2-Epoxypropane → HCID 66878072, compound

HRID 633209Notes

Reaction equation

HRID 633209 reaction equation
[CH2:1]1[O:4][C@@H:2]1[CH3:3].[SH:5][C:6]1[CH:15]=[CH:14][C:9]([C:10]([O:12][CH3:13])=[O:11])=[CH:8][CH:7]=1>>[OH:4][C@H:2]([CH3:3])[CH2:1][S:5][C:6]1[CH:7]=[CH:8][C:9]([C:10]([O:12][CH3:13])=[O:11])=[CH:14][CH:15]=1

Participants

3

Reactant 2

HCID 146261(R)-1,2-EpoxypropaneHCID 237573Methyl 4-sulfanylbenzoate

Product 1

HCID 66878072HCID 66878072, compound

Procedure

100 mg of (R)-propylene oxide′ was reacted with methyl 4-mercaptobenzoate via Procedure S to afford (R)-methyl 4-(2-hydroxypropylthio)benzoate. 169 mg of (R)-methyl 4-(2-hydroxypropylthio)benzoate was reacted via Procedure R to give (R)-methyl 4-(2-hydroxypropylsulfonyl)benzoate. 179 mg of (R)-methyl 4-(2-hydroxypropylsulfonyl)benzoate was hydrolyzed via Procedure M to give (R)-4-(2-hydroxypropylsulfonyl)benzoic acid. 45 mg of 4-chloro-3-(pyridine-2-yl)aniline was coupled to (R)-4-(2-hydroxypropylsulfonyl)benzoic acid via Procedure G. The product was purified on reverse phase HPLC to yield (R)—N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(2-hydroxypropylsulfonyl)benzamide. MS (Q1) 431.2 (M)+.

Sources & evidence

ORD record
ord-4dea0eac9f1f4ceebaa45513a34a231c
Source dataset
uspto-grants-2016_04
Patent number
US09321761B2

Reaction notes

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