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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292718Generated: October 25, 2026

Mitomycin C → Mitomycin C

https://huagongshe.com/reaction/1292718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMitomycin CHCID 5746—
SolventDimethylformamideHCID 6228—
ProductMitomycin CHCID 5746—
Product2-DimethylaminopyridineHCID 21885—

Reaction Steps

A solution of mitomycin C (MMC, 0.35 mmol), dimethylaminopyridine (0.1 mmol) and dimethylformamide (DMF, 2 mL) was prepared. The MMC solution was slowly added to the acyl chloride solution. After overnight reaction, the methylene chloride was evaporated off and the crude product was recovered by addition of isopropanol followed by filtration. The mPEG-DTB-MMC conjugate was further purified by two precipitation from ethanol. Yield: 3.4 g. The MMC content (≈90%) was determined by UV. The conjugate was further characterized by 1H NMR (360 MHz, CDCl3): δ 1.18 (d, J=7.5, 3H), 1.76 (s, 3H), 2.96–3.03 (m, 3H), 3.19 (s, 3H), 3.29 (dd, J=4.7 and 2.9 Hz, 1H), 3.41 (dd, J=5.0 and 2.2 Hz, 1H), 3.48 (dd, J=13.7 and 2.5 Hz, 1H), 3.60 (s, PEG, 1000H), 4.15 (t, OCOCH2, 2H), 4.27–4.36 (m, 2H), 4.43 (d, J=13.3 Hz, 1H), 4.61 (s, 2H), 4.90 (ddd, J=10.4 and 5.0 and 2.2 Hz, 1H), 5.00 (s, 2H), 7.32 (d, J=8.6 Hz, 2H), 7.50 (d, J=7.9 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238368B2
Source datasetuspto-grants-2007_07
ORD IDord-41075eb82baf41f48ee5c2617b5d4e03
Source noteuspto-grants-2007_07