Ethyl acetate hexane → HCID 68712714, compound

HRID 1787261Notes

Reaction equation

HRID 1787261 reaction equation
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([C@H:10]2[C:14]3[C:15]([CH3:28])=[C:16]([NH:20][C:21](=[O:27])[CH2:22][C:23]([CH3:26])([CH3:25])[CH3:24])[C:17]([CH3:19])=[CH:18][C:13]=3[O:12][CH2:11]2)=[CH:6][CH:5]=1)([CH3:3])[CH3:2].CCCCCC.[C:35](OCC)(=[O:37])[CH3:36]>C(Cl)(Cl)Cl>[C:35]([C:18]1[C:13]2[O:12][CH2:11][C@@H:10]([C:7]3[CH:6]=[CH:5][C:4]([CH:1]([CH3:2])[CH3:3])=[CH:9][CH:8]=3)[C:14]=2[C:15]([CH3:28])=[C:16]([NH:20][C:21](=[O:27])[CH2:22][C:23]([CH3:26])([CH3:25])[CH3:24])[C:17]=1[CH3:19])(=[O:37])[CH3:36]

Participants

4

Procedure

Using N-((3S)-3-(4-isopropylphenyl)-4,6-dimethyl-2,3-dihydro-1-benzofuran-5-yl)-3,3-dimethylbutanamide obtained in Example 71, the title compound was synthesized in the same manner as in Example 38. Yield: 46%. Melting point: 177-178° C. (hexane-ethyl acetate). [α]D20=−6.0° (c=0.510, chloroform).

Sources & evidence

ORD record
ord-8622227d8ca64372aa4c2f1ce39b1f04
Source dataset
uspto-grants-2009_03
Patent number
US07507841B2

Reaction notes

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