Pyrrolidine → HCID 59750615, compound

HRID 747882Notes

Reaction equation

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

Participants

Reactant 2

HCID 31268Pyrrolidine

HCID 11592086HCID 11592086, compound

Product 1

HCID 59750615HCID 59750615, compound

Procedure

The title product was prepared as a white solid according to the procedure described in Example 34 using 5-[2-[4-(2-chloro-ethoxy)-phenyl]-4-methyl-7-(2-trimethylsilanyl-ethoxymethoxy)-2H-chromen-3-yl]-2-methoxy-pyridine and pyrolidine as the starting material.

Sources & evidence

ORD record: ord-028cecafc460449e9eaf75b96f515992
Source dataset: uspto-grants-2008_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07399767B2

Reaction notes

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