HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408300Generated: November 2, 2026
Diisopropylcarbodiimide → HCID 86704391, compound
https://huagongshe.com/reaction/1408300
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | 2-(2-(2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)ethoxy)ethoxy)acetic acid | HCID 2756092 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86704391 | HCID 86704391 | — |
Reaction Steps
2-[2-(2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}ethoxy)ethoxy]acetic acid (185 mg, 0.480 mmol) and N-hydroxysuccinimide (110 mg, 0.956 mmol) were dissolved in anhydrous THF (1.5 mL). DIC was added dropwise to the solution at r.t., leading to the precipitation of a white solid. After 2 h, the reaction mixture was filtrated through a PTFE membrane filter (0.2 μm), and the solvent was removed. The crude product was redissolved in Et2O. The organic phase was washed with aq. NaHCO3 and 0.5 M aq. HCl. The organic layer was dried over Na2SO4, and the solvent was removed. The crude product was dissolved in CH2Cl2, and the solution was filtrated. After removal of the solvent, the crude product 39 (210 mg) was used in the synthesis of 40 without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921328B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-d5d8c9c9c6c941a99efc6218c7e2607b |
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| Source note | uspto-grants-2014_12 |
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