(1,4-Dimethyl-1H-indazol-5-yl)boronic acid → HCID 86720142, compound

HRID 2408569Notes

Reaction equation

HRID 2408569 reaction equation
[CH3:1][O:2][C:3](=[O:26])[CH2:4][C@H:5]1[C:9]2[CH:10]=[CH:11][C:12]([O:14][C@H:15]3[C:23]4[C:18](=[C:19]([OH:25])[CH:20]=[CH:21][C:22]=4[F:24])[CH2:17][CH2:16]3)=[CH:13][C:8]=2[O:7][CH2:6]1.[CH3:27][N:28]1[C:36]2[C:31](=[C:32]([CH3:40])[C:33](B(O)O)=[CH:34][CH:35]=2)[CH:30]=[N:29]1>>[CH3:1][O:2][C:3](=[O:26])[CH2:4][C@H:5]1[C:9]2[CH:10]=[CH:11][C:12]([O:14][C@H:15]3[C:23]4[C:18](=[C:19]([O:25][C:33]5[C:32]([CH3:40])=[C:31]6[C:36](=[CH:35][CH:34]=5)[N:28]([CH3:27])[N:29]=[CH:30]6)[CH:20]=[CH:21][C:22]=4[F:24])[CH2:17][CH2:16]3)=[CH:13][C:8]=2[O:7][CH2:6]1

Participants

3

Procedure

The title compound is prepared from {(S)-6-[(R)-7-fluoro-4-hydroxy-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester and 1,4-dimethyl-indazole-5-boronic acid following a procedure analogous to that described for Intermediate 6. LC (method 10): tR=0.88 min; Mass spectrum (ESI+): m/z=503 [M+H]+.

Sources & evidence

ORD record
ord-55154197b2e84e258fb80c600afa5f9e
Source dataset
uspto-grants-2014_08
Patent number
US08815864B2

Reaction notes

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