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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305998Generated: October 25, 2026

Dicyclohexylcarbodiimide → N-Hydroxysulfosuccinimide

https://huagongshe.com/reaction/2305998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactantsodium N-hydroxysulfosuccinimideHCID 86222747—
SolventDimethylacetamideHCID 31374—
ProductN-HydroxysulfosuccinimideHCID 133909—

Reaction Steps

L-DM1-TPA (6, 2 mg 0.002 mmol) was dissolved in dimethylacetamide (0.25 mL), to which N-hydroxysulfosuccinimide sodium salt (1.0 mg, 0.0046 mmol) and dicyclohexylcarbodiimide (1.0 mg, 0.0048 mmol) were added. After 3 hours, 0.5 mL of diisopropyl alcohol was added and the resulting precipitate was removed by filtration. HPLC analysis (Vydac C-18 column, 10×250 C18 column, 30° C., flow rate 4.75 mL/min, 50 mM triethylammonium formate pH 3.8 buffer with a linear methanol gradient (30% to 90% over 30 minutes) of the filtrate showed two major peaks, one for unreacted L-DM1-TPA at 22 min and one for L-DM1-TPA sulfosuccinimidyl ester at 19 min. The compound eluting at 19 min was isolated and analyzed by mass spectrometry showing that it had the expected peak consistent with the disodiated molecular ion (M++2Na) of 3a, m/e 1091.4. Further fragmentation of the 1091.4 ion gave predictable daughter ions, m/e 1073.4 (M++2Na—H2O ), 874.4 (M++2Na-sodiated N-hydroxysulfosuccinimide).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441163B1
Source datasetuspto-grants-2002_08
ORD IDord-ec2c358087bc4087aae8386a56e38454
Source noteuspto-grants-2002_08