HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 11312262, compound → HCID 11242358, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 11312262 | HCID 11312262 | — |
| Reactant | HCID 11380547 | HCID 11380547 | — |
| Product | HCID 11242358 | HCID 11242358 | 52% |
Reaction Steps
The compound was synthesized in 52% yield according to the procedure described for the synthesis of (7-dimethylsulfamoyl-benzimidazol-1-yl)-acetic acid, part C, starting from 2-{[2-nitro-6-(propylsulfonyl)phenyl]amino}ethanol. MS (ESI) m/z 259 [M+H]. 1H NMR (400 MHz, CDCl3/CD3OD) δ ppm 1.00 (t, J=7.3 Hz, 3H), 1.82-1.72 (m, 2H), 3.15-3.11 (m, 2H), 3.29-3.27 (m, 2H), 3.80-3.77 (m, 2H), 6.92-6.90 (m, 1H), 6.96 (t, J=7.8 Hz, 1H), 7.23 (dd, J=7.7, 1.6 Hz, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07645784B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-f6262a143caa45ae8e109d97b0b47089 |
| Source note | uspto-grants-2010_01 |