Isopropyl iodide → HCID 22311308, compound

HRID 491449Notes

Reaction equation

I[CH:2](C)C.[ClH:5].[CH3:6][O:7][C:8]1[CH:9]=[C:10]([C:16]2[C@@H:25]3[C@@H:20]([CH2:21][CH:22]=[CH:23][CH2:24]3)[C:19](=[O:26])[N:18]([CH:27]3[CH2:32][CH2:31][N:30]([CH2:33][C:34]4C=C5C(C=CC(=O)O5)=CC=4)[CH2:29][CH2:28]3)[N:17]=2)[CH:11]=[CH:12][C:13]=1[O:14][CH3:15]>>[ClH:5].[CH3:6][O:7][C:8]1[CH:9]=[C:10]([C:16]2[CH:25]3[CH:20]([CH2:21][CH:22]=[CH:23][CH2:24]3)[C:19](=[O:26])[N:18]([CH:27]3[CH2:32][CH2:31][N:30]([CH:33]([CH3:34])[CH3:2])[CH2:29][CH2:28]3)[N:17]=2)[CH:11]=[CH:12][C:13]=1[O:14][CH3:15]

Participants

Reactant 2

HCID 6362Isopropyl iodide

HCID 86601097HCID 86601097, compound

Product 1

HCID 22311308HCID 22311308, compound

Procedure

Prepared from 2-iodopropane and starting compound A1 as described for compound 18. M.p. 158-159° C.

Sources & evidence

ORD record: ord-d22485486a2949ee878ee6cbfdd81971
Source dataset: uspto-grants-2009_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07531540B2

Reaction notes

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