2-[2-(4-Amino-phenoxy)-phenoxy]-2-methyl-propionic acid tert-butyl ester → HCID 22179538, compound

HRID 1796630Notes

Reaction equation

HRID 1796630 reaction equation
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([O:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[C:8]([CH:17]=1)[CH2:9][O:10][CH:11]1[CH2:16][CH2:15][CH2:14][CH2:13][O:12]1)([O-])=O.C(OC(=O)C(OC1C=CC=CC=1OC1C=CC(N)=CC=1)(C)C)(C)(C)C>>[O:18]([C:7]1[CH:6]=[CH:5][C:4]([NH2:1])=[CH:17][C:8]=1[CH2:9][O:10][CH:11]1[CH2:16][CH2:15][CH2:14][CH2:13][O:12]1)[C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1

Participants

3

Reactant 2

HCID 210251742-[2-(4-Amino-phenoxy)-phenoxy]-2-methyl-propionic acid tert-butyl esterHCID 221794762-(5-Nitro-2-phenoxy-benzyloxy)-tetrahydro-pyran

Product 1

HCID 22179538HCID 22179538, compound

Procedure

Compound 394D was prepared from 394C in quantitative yield by a route analogous to that used for the preparation of compound 388C.

Sources & evidence

ORD record
ord-ca529bf535c84ec0a608e3603658445f
Source dataset
uspto-grants-2006_04
Patent number
US07030112B2

Reaction notes

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