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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266043Generated: November 2, 2026

Dimethylformamide → HCID 178454171, compound

https://huagongshe.com/reaction/266043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl AcetateHCID 8857—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBoc-His(Boc)-OHHCID 7023100—
ProductHCID 178454171HCID 17845417138%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650407
Source datasetuspto-grants-1997_07
ORD IDord-0e224ec522dd489094eb7e13a51b04c7
Source noteuspto-grants-1997_07