2-[(2-Methylpropoxy)methyl]oxirane → HCID 57661955, compound

HRID 1665371Notes

Reaction equation

HRID 1665371 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.[CH2:22]([O:26][CH2:27][CH:28]1[CH2:30][O:29]1)[CH:23]([CH3:25])[CH3:24]>>[OH:29][CH:28]([CH2:27][O:26][CH2:22][CH:23]([CH3:25])[CH3:24])[CH2:30][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

Participants

3

Reactant 2

HCID 981552-[(2-Methylpropoxy)methyl]oxiraneHCID 57661820Spiro[naphtho[1,2-b][1,4]oxathiine-2,4'-piperidine]-5,6-dione

Product 1

HCID 57661955HCID 57661955, compound

Procedure

Compound 174 was synthesized using spiro[naphtho[1,2-b][1,4]oxathiine-2,4′-piperidine]-5,6-dione, 2-(isobutoxymethyl)oxirane and conditions outlined in procedure X. LCMS: 432 [M+H]; Rt=0.97 min.

Sources & evidence

ORD record
ord-d659b023308f458aafe9f2829f65edda
Source dataset
uspto-grants-2011_10
Patent number
US08039503B2

Reaction notes

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