HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724719Generated: October 30, 2026
O-Phenylenediamine → HCID 11534745, compound
https://huagongshe.com/reaction/724719
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | HCID 11633706 | HCID 11633706 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11534745 | HCID 11534745 | 82% |
Reaction Steps
A solution of (2S)-2-[(benzyloxy)carbonyl]amino-3-[4-(1,1-dioxido-3-oxoisothiazolidin-5-yl)-3-methylphenyl]propanoic acid (200 mg, 0.448 mmol) in N,N-dimethylformamide (2.0 mL) was treated with benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (0.218 g, 0.493 mmol). After stirring for 10 minutes at 0° C., a solution of 1,2-benzenediamine (72.7 mg, 0.672 mmol) and N,N-diisopropylethylamine (0.39 mL, 2.24 mmol) in DMF (1.0 mL) was cannulated into the reaction flask. The solution was stirred at 25° C. for 2 h. The solution was diluted with ethyl acetate, washed with saturated aqueous sodium bicarbonate solution and 1.0 M hydrochloric acid solution. The organic phase was dried over sodium sulfate, filtered, and concentrated in vacuo. The crude residue was purified by preparative LCMS to yield the desired product (196 mg, 82%). 1H NMR (400 MHz, CD3OD): δ 7.47 (d, 0.5H), 7.39–7.22 (m, 9H), 7.12 (d, 0.5H), 7.07 (s, 1H), 6.82 (d, 0.5H), 6.71 (d, 0.5H), 5.50 (t, 1H), 5.10 (s, 2H), 4.47 (m, 1H), 3.3 (m, 2H), 3.07 (m, 2H), 2.48 (s, 1.5H), 2.38 (s, 1.5H); MF=C27H28N4O6S; LCMS found for C27H29N4O6S (M+H)+: m/z=537.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07141596B2 |
|---|
| Source dataset | uspto-grants-2006_11 |
|---|
| ORD ID | ord-19f5f03035404887812ca35bd36f5ee0 |
|---|
| Source note | uspto-grants-2006_11 |
|---|