7N-646S → HCID 22280137, compound

HRID 1063752Notes

Reaction equation

HRID 1063752 reaction equation
Cl[CH2:2][C:3]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[Cl:14])[O:5][N:4]=1.C[O:16][C:17](=[O:30])[CH2:18][O:19][C:20]1[CH:28]=[CH:27][C:26]([SH:29])=[C:25]2[C:21]=1[CH2:22][CH2:23][CH2:24]2>>[Cl:14][C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=1[C:6]1[O:5][N:4]=[C:3]([CH2:2][S:29][C:26]2[CH:27]=[CH:28][C:20]([O:19][CH2:18][C:17]([OH:30])=[O:16])=[C:21]3[C:25]=2[CH2:24][CH2:23][CH2:22]3)[CH:7]=1

Participants

3

Reactant 2

HCID 14847677N-646SHCID 20770872(7-Mercapto-indan-4-yloxy)-acetic Acid Methyl Ester

Product 1

HCID 22280137HCID 22280137, compound

Procedure

The title compound was prepared in the manner analogous to Example 1F using commercially available 3-chloromethyl-5-(2-chloro-phenyl)-isoxazole and 12C. MS m/z 430 (M+1).

Sources & evidence

ORD record
ord-19a4d5a3704c4fd1a25b83d09ddf190b
Source dataset
uspto-grants-2005_11
Patent number
US06964983B2

Reaction notes

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