(S)-(-)-1-Phenylethyl isocyanate → HCID 66578545, compound

HRID 1528724Notes

Reaction equation

HRID 1528724 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:12][N:11]=[C:10]([CH3:13])[C:9]=2[CH2:14][OH:15])=[CH:4][CH:3]=1.[CH3:16][C@H:17]([N:24]=[C:25]=[O:26])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[O:12][N:11]=[C:10]([CH3:13])[C:9]=2[CH2:14][O:15][C:25](=[O:26])[NH:24][C@H:17]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH3:16])=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 2724173(S)-(-)-1-Phenylethyl isocyanateHCID 58218538[5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-yl]-methanol

Product 1

HCID 66578545HCID 66578545, compound

Procedure

Prepared according to the procedure described in Example 19, Step 2, using [5-(4-bromo-phenyl)-3-methyl-isoxazol-4-yl]-methanol and (S)-(−)-α-methylbenzyl isocyanate.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-63f9e512808b43daa85ddd7f5c43db1d
Source dataset
uspto-grants-2015_07
Patent number
US09090573B2

Reaction notes

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