HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-[1,3]thiazolo[5,4-b]pyridin-2-amine → 2-(2,6-Dichlorophenyl)-1H-indole-6-carboxylic acid (5-bromothiazolo[5,4-b]pyridin-2-yl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-[1,3]thiazolo[5,4-b]pyridin-2-amine | HCID 45789977 | — |
| Reactant | 2-(2,6-dichlorophenyl)-1H-indole-6-carboxylic acid | HCID 66966053 | — |
| Product | 2-(2,6-Dichlorophenyl)-1H-indole-6-carboxylic acid (5-bromothiazolo[5,4-b]pyridin-2-yl)-amide | HCID 86651268 | — |
Reaction Steps
The title compound was prepared from 2-(2,6-dichlorophenyl)-1H-indole-6-carboxylic acid and 5-bromothiazolo[5,4-b]pyridin-2-ylamine (WO 2007041365) analogous to Example 3-11. 1H NMR (DMSO-d6, 400 MHz): δ 13.08 (s, broad, 1H), 12.01 (s, broad, 1H) 8.33 (s, 1H), 8.11 (d, J=8.5 Hz, 1H), 7.86 (dd, J=8.5, 1.5 Hz, 1H), 7.71 (m, 4H), 7.56 (m, 1H), 6.65 (d, J=1.3 Hz, 1H). MS (m/z) 518.9 (M+1), Retention time=1.58 min (Method 10). High Res. MS: theory 516.9292; measured 516.9277.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08222248B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-c20e111f680541dcbab8d5cc0b72afd5 |
| Source note | uspto-grants-2012_07 |