HCID 11074770, compound → HCID 58904459, compound

HRID 1292745Notes

Reaction equation

[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:27]=[C:28]([O:30][CH3:31])[CH:29]=1)[O:6][C@@H:7]([C@:11]1([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:14][CH2:13][NH:12]1)[C:8]([OH:10])=[O:9].[CH3:32][O:33][C:34]1[CH:35]=[C:36]([CH2:42][C:43](Cl)=[O:44])[CH:37]=[C:38]([O:40][CH3:41])[CH:39]=1>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:27]=[C:28]([O:30][CH3:31])[CH:29]=1)[O:6][C@@H:7]([C@:11]1([C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:14][CH2:13][N:12]1[C:43](=[O:44])[CH2:42][C:36]1[CH:35]=[C:34]([O:33][CH3:32])[CH:39]=[C:38]([O:40][CH3:41])[CH:37]=1)[C:8]([OH:10])=[O:9]

Participants

Reactant 2

HCID 11074770HCID 11074770, compound

HCID 58904496HCID 58904496, compound

Product 1

HCID 58904459HCID 58904459, compoundYield 60.2%

Procedure

(±)-(S*)-(3,5-dimethoxy-phenoxy)-{(1S*)-2-[2-(3,5-dimethoxy-phenyl)-acetyl]-1-phenyl-1,2,3,4-tetrahydro-isoquinolin-1-yl}-acetic acid (77 mg) is prepared in analogy to Example 5 starting from (±)-(S*)-(3,5-dimethoxy-phenoxy)-((1S*)-1-phenyl-1,2,3,4-tetrahydro-isoquinolin-1-yl)-acetic acid (90 mg, 0.214 mmol, Example 1) and 3,5-dimethoxyphenylacetyl chloride (83 mg, 0.385 mmol). LC-MS2: tR=5.23 min, [M+1]+=598.35, [M−1]−=596.29.

Sources & evidence

ORD record: ord-ba1d5fbdf1c24b699ac9396c60b0e0cf
Source dataset: uspto-grants-2007_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07238685B2

Reaction notes

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