1-Iodopropane → HCID 58990132, compound

HRID 2261910Notes

Reaction equation

[C:1]([O:5][C:6]([NH:8][C:9]([C:18]1[O:22][C:21]([C:23]2[CH:24]=[C:25]([CH:29]=[C:30]([N:32]([CH3:37])[S:33]([CH3:36])(=[O:35])=[O:34])[CH:31]=2)[C:26]([OH:28])=[O:27])=[N:20][N:19]=1)([CH3:17])[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:38](I)[CH2:39]C>>[C:1]([O:5][C:6]([NH:8][C@:9]([C:18]1[O:22][C:21]([C:23]2[CH:24]=[C:25]([CH:29]=[C:30]([N:32]([CH2:37][CH2:38][CH3:39])[S:33]([CH3:36])(=[O:34])=[O:35])[CH:31]=2)[C:26]([OH:28])=[O:27])=[N:20][N:19]=1)([CH3:17])[CH2:10][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

Reactant 2

HCID 336431-Iodopropane

HCID 68707669HCID 68707669, compound

Product 1

HCID 58990132HCID 58990132, compound

Procedure

Prepared using a procedure similar to that employed for the synthesis of Intermediate VI, substituting propyl iodide in the place of methyl iodide in Step B of the Intermediate III synthesis.

Workup

customPrepared

Sources & evidence

ORD record: ord-784e680136ab4d258e71e6b7efec86c4
Source dataset: uspto-grants-2010_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07847100B2

Reaction notes

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