HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indol-6-ylboronic acid → HCID 136027570, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indol-6-ylboronic acid | HCID 2763205 | — |
| Reactant | HCID 68487682 | HCID 68487682 | — |
| Product | HCID 136027570 | HCID 136027570 | — |
Reaction Steps
The titled compound was prepared in a manner analogous to Example 69, steps C-E, using 1-[6-iodo-4-oxo-3-(2-trimethylsilanyl-ethoxymethyl)-3,4-dihydro-quinazolin-2-yl]-1H-pyrazole-4-carboxylic acid ethyl ester (Example 69 product from step B) and indole-6-boronic acid in step C. MS (ESI): mass calcd. for C20H13N5O3, 371.1; m/z found, 372.1 [M+H]+. 1H NMR (600 MHz, DMSO-d6): 13.01 (s, 1H), 12.86 (s, 1H), 11.23 (s, 1H), 8.99 (s, 1H), 8.37 (s, 1H), 8.27 (s, 1H), 8.20 (s, 1H), 7.77 (s, 2H), 7.67 (d, J=8.2 Hz, 1H), 7.43 (s, 2H), 6.48 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08937078B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-c15608f662294d2399e1614bcb4182af |
| Source note | uspto-grants-2015_01 |