HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane methanol ammonium hydroxide → HCID 44235509, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane methanol ammonium hydroxide | HCID 21896990 | — |
| Reactant | HCID 66850407 | HCID 66850407 | — |
| Product | HCID 44235509 | HCID 44235509 | — |
Reaction Steps
3-[3-(2-Methyl-pyridin-4-yl)-1H-indole-6-carbonyl]-benzenesulfonamide is prepared from 0.25 g of 5-[3-bromo-1-(tert-butyl-dimethyl-silyl)-1H-indole-6-carbonyl]-N-(tert-butyl-dimethyl-silyl)-benzenesulfonamide according to the procedure described in Example 6 (microwave irradiation at 150° C. for 5 min). MS (m/z): 390 (M−1); Rf 0.19 (90:10:1 methylene chloride/methanol/ammonium hydroxide)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08975439B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-5e38055d675f4ef49994d5e31267ec2c |
| Source note | uspto-grants-2015_03 |