ethyl (4'-bromo-6,6-dimethyl-2'-oxo-5,6-dihydrospiro[benzo[1,2-b:5,4-b']difuran-3,3'-indol]-1'(2'H)-yl)acetate → (4'-bromo-6,6-dimethyl-2'-oxo-5,6-dihydrospiro[benzo[1,2-b:5,4-b']difuran-3,3'-indol]-1'(2'H)-yl)acetic acid

HRID 645194Notes

Reaction equation

HRID 645194 reaction equation
C([O:3][C:4](=[O:30])[CH2:5][N:6]1[C:14]2[C:9](=[C:10]([Br:15])[CH:11]=[CH:12][CH:13]=2)[C:8]2([CH2:19][O:18][C:17]3[CH:20]=[C:21]4[C:25](=[CH:26][C:16]2=3)[CH2:24][C:23]([CH3:28])([CH3:27])[O:22]4)[C:7]1=[O:29])C.C(OC(=O)CN1C2C(=CC=CC=2)C2(C3=CC4OCOC=4C=C3OC2)C1=O)C>>[Br:15][C:10]1[CH:11]=[CH:12][CH:13]=[C:14]2[C:9]=1[C:8]1([CH2:19][O:18][C:17]3[CH:20]=[C:21]4[C:25](=[CH:26][C:16]1=3)[CH2:24][C:23]([CH3:28])([CH3:27])[O:22]4)[C:7](=[O:29])[N:6]2[CH2:5][C:4]([OH:30])=[O:3]

Participants

3

Procedure

Following the procedure as described in EXAMPLE 2, and making non-critical variations using ethyl(4′-bromo-6,6-dimethyl-2′-oxo-5,6-dihydrospiro[benzo[1,2-b:5,4-b′]difuran-3,3′-indol]-1′(2′H)-yl)acetate to replace ethyl(2′-oxospiro[furo[2,3-f][1,3]benzodioxole-7,3′-indol]-1′(2′H)-yl)acetate, the title compound was obtained. The product was used directly in the next step.

Sources & evidence

ORD record
ord-2d4c6eb7a52a4556bd97944bd357b1c5
Source dataset
uspto-grants-2010_04
Patent number
US07700641B2

Reaction notes

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