Ethyl acetate hexane → HCID 86612352, compound

HRID 1787239Notes

Reaction equation

HRID 1787239 reaction equation
[C:1]([NH:5][C:6]([NH:8][C:9]1[C:10]([CH3:28])=[CH:11][C:12]2[O:16][CH2:15][C@H:14]([C:17]3[CH:22]=[CH:21][C:20]([CH:23]([CH3:25])[CH3:24])=[CH:19][CH:18]=3)[C:13]=2[C:26]=1[CH3:27])=[O:7])([CH3:4])([CH3:3])[CH3:2].[C:29](OCC)(=[O:31])C.CCCCCC>C(Cl)(Cl)Cl>[C:1]([NH:5][C:6]([NH:8][C:9]1[C:10]([CH3:28])=[C:11]([CH:29]=[O:31])[C:12]2[O:16][CH2:15][C@H:14]([C:17]3[CH:18]=[CH:19][C:20]([CH:23]([CH3:24])[CH3:25])=[CH:21][CH:22]=3)[C:13]=2[C:26]=1[CH3:27])=[O:7])([CH3:2])([CH3:3])[CH3:4]

Participants

4

Procedure

Using (+)-N-(tert-butyl)-N′-((3R)-3-(4-isopropylphenyl)-4,6-dimethyl-2,3-dihydro-1-benzofuran-5-yl)urea, the title compound was synthesized in the same manner as in Example 20. Yield: 78%. Melting point: 209-210° C. (ethyl acetate-hexane). [α]D20=−31.2° (c=0.48, chloroform).

Sources & evidence

ORD record
ord-abe2a1165afd4a07b0f80d4a45a490bb
Source dataset
uspto-grants-2009_03
Patent number
US07507841B2

Reaction notes

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