HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266043Generated: November 2, 2026
Dimethylformamide → HCID 178454171, compound
https://huagongshe.com/reaction/266043
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Boc-His(Boc)-OH | HCID 7023100 | — |
| Product | HCID 178454171 | HCID 178454171 | 38% |
Reaction Steps
A mixture of Boc-His(Boc)-OH (506 mg, 1.42 mmol), Compound I-5 (418 mg, 0.92 mmol) and DCC (195 mg, 0.96 mmol) in CE2Cl2 /DMF (1:1, 2.4 mL) was stirred 12 hours at ambient temperature. The reaction mixture was diluted with ethyl acetate (25 mL) and filtered. The ethyl acetate layer was washed with a 2% NaHCO3 solution (2×20 mL), saturated NaCl solution (1×20 mL) and dried (MgSO4). Petroleum ether was added and a yellowish-green precipitate was collected. Purification by column chromatography (silica gel; EtOAc; Rf=0.4) gave 154 mg, (38%) of the Boc-Histidine(Boc) ester as a white solid. 1H NMR (DMSO-d6) δ 1.35 (s, 9H, tBu), 1.48 (s, 9H, tBu). A solution of the product from Example-9 step-1 (144 mg) in EtOAc (2 mL) was added 4N mL). The mixture was stirred for 2 h at room temperature, diluted with water (30 mL) and extracted with EtOAc (1×30 mL) and ether (1×30 mL). The aqueous layer was lyophilized to give a solid product ester (105 mg, 86%), mp 228° C. (dec.), MS m/z=592 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05650407 |
|---|
| Source dataset | uspto-grants-1997_07 |
|---|
| ORD ID | ord-0e224ec522dd489094eb7e13a51b04c7 |
|---|
| Source note | uspto-grants-1997_07 |
|---|