HCID 131719468, compound → HCID 22862708, compound

HRID 1735796Notes

Reaction equation

HRID 1735796 reaction equation
[NH2:1][C:2]1[C:10]([CH2:11]/[CH:12]=[C:13]2/[C@H:14]([CH2:19][C:20]([OH:22])=[O:21])[CH2:15]CC[CH2:18]/2)=[C:9]([O:23][CH3:24])[C:8]([CH3:25])=[C:7]2[C:3]=1[C:4](=[O:26])[O:5][CH2:6]2>C(OC)(C)(C)C>[NH2:1][C:2]1[C:10]([CH2:11]/[CH:12]=[C:13](\[CH3:18])/[CH:14]([CH3:15])[CH2:19][C:20]([OH:22])=[O:21])=[C:9]([O:23][CH3:24])[C:8]([CH3:25])=[C:7]2[C:3]=1[C:4](=[O:26])[O:5][CH2:6]2

Participants

3

Procedure

(E)-2-[2-[2-[4-amino-1,3-dihydro-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl]ethylidene]cyclohex-1(S)-yl]acetic acid, mp 175°-177° C. (tert butylmethyl ether); and

Sources & evidence

ORD record
ord-c4e4a1648e57420983d465aaeab52f2c
Source dataset
uspto-grants-1996_07
Patent number
US05538969

Reaction notes

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