Homoallyl bromide → HCID 57661879, compound

HRID 1665341Notes

Reaction equation

HRID 1665341 reaction equation
[NH:1]1[CH2:6][CH2:5][C:4]2([O:11][C:10]3[C:12]4[C:17]([C:18](=[O:21])[C:19](=[O:20])[C:9]=3[S:8][CH2:7]2)=[CH:16][CH:15]=[CH:14][CH:13]=4)[CH2:3][CH2:2]1.Br[CH2:23][CH2:24][CH:25]=[CH2:26]>>[CH2:26]([N:1]1[CH2:2][CH2:3][C:4]2([O:11][C:10]3[C:12]4[C:17]([C:18](=[O:21])[C:19](=[O:20])[C:9]=3[S:8][CH2:7]2)=[CH:16][CH:15]=[CH:14][CH:13]=4)[CH2:5][CH2:6]1)[CH2:25][CH:24]=[CH2:23]

Participants

3

Reactant 2

HCID 21241Homoallyl bromideHCID 57661820Spiro[naphtho[1,2-b][1,4]oxathiine-2,4'-piperidine]-5,6-dione

Product 1

HCID 57661879HCID 57661879, compound

Procedure

Compound 143 was synthesized using spiro[naphtho[1,2-b][1,4]oxathiine-2,4′-piperidine]-5,6-dione, 4-bromobut-1-ene and conditions outlined in procedure V. LCMS: 356 [M+H]; Rt=0.88 min.

Sources & evidence

ORD record
ord-482d05c7aab14cf2be1f35f28ecf4756
Source dataset
uspto-grants-2011_10
Patent number
US08039503B2

Reaction notes

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