HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656351Generated: October 29, 2026
Dichloromethane → HCID 59718448, compound
https://huagongshe.com/reaction/656351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 131729305 | HCID 131729305 | — |
| Product | HCID 59718448 | HCID 59718448 | — |
Reaction Steps
To a solution of Fmoc-Cys(SStBu)-OH (1, 2.15 g, 5.0 mmole) dissolved in anhydrous CH2Cl2 (30 mL) was added N-Ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDAC, 1.146 g, 6 mmole), the reaction mixture was stirred for 10 min. at room temperature (RT) and then added N-hydroxysuccinimide (NHS) (0.690 g, 6.0 mmole). To this reaction mixture was added catalytic amount of N,N′-dimethlyaminopyridine and stirred at RT until completion of reaction tested with TLC. The solvent was evaporated and the residue obtained was extracted with ethyl acetate (50 mL×2), washed with 1M NaHCO3 (10 mL), followed by brine solution (20 mL) and dried over anhydrous Na2SO4. Evaporation of the solvent afforded 2 as a white crystalline solid. Yield. 2.5 g (95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071755B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-5138bdc3206b4759b852bbc05667efc8 |
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| Source note | uspto-grants-2011_12 |
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