HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-5-bromopyridine → HCID 57718225, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-5-bromopyridine | HCID 70622 | — |
| Reactant | Benzenesulfonyl chloride, 2,4-dichloro- | HCID 204419 | — |
| Reactant | 4-(N-piperidinylsulfonyl)thiophenol | HCID 57718290 | — |
| Product | HCID 57718225 | HCID 57718225 | — |
Reaction Steps
Prepared from 2-amino-5-bromopyridine and 4-(N -piperidinylsulfonyl)thiophenol according to General Method 11 step 1 followed by reaction with 2,4-dichlorophenylsulfonyl chloride according to General Method 11 step 2. 1H NMR (CDCl3): 11.95 (1 H, br s, NH), 8.55 (1 H, s, Ar CH ortho to 2×Cl), 8.29 (1 H, d, CH ortho to SO2NH), 7.85, 7.61, 7.54 & 7.39 (4×1 H, d, s, d & d, J 11, 10 & 11 Hz, A- & B-ring CH's) 7.73 & 7.30 (2×2 H, 2×d, 2×J 10 Hz, Ar CH's of C-ring), 3.10-3.01 (4H, m, CH2NCH2), 2.18 (3H, s, CH3), 1.79-1.68 (4 H, m, CH2CH2CH2CH2CH2), 1.60-1.48 (2 H, m, CH2CH2CH2CH2CH2). Hplc (Luna 2, Gradient 5): rt=6.48 minutes. LC/MS rt=7.19 minutes, 558/560 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893077B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-bd07228731d54551a3f67a1d464069f6 |
| Source note | uspto-grants-2011_02 |