HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557463Generated: October 29, 2026
4-Iodobenzenesulfonyl chloride → HCID 69002742, compound
https://huagongshe.com/reaction/557463
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Iodobenzenesulfonyl chloride | HCID 7399 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 86622258 | HCID 86622258 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69002742 | HCID 69002742 | 80% |
Reaction Steps
In a round bottom flask 2-[3-(5-Amino-1-carboxy-pentyl)-ureido]-pentanedioic acid di t-butyl ester (300 mg, 0.62 mmol) is suspended in water (10 mL) and 1,4 dioxane (10 mL) and TEA (1.75 mL, 1.25 mmol) was added followed by 4-iodo-benzenesulfonyl chloride and the mixture stirred overnight at 50° C. The reaction mixture was evaporated to dryness, taken up in DCM and chromatographed over silica gel to afford the desired product (375 mg, 80%) as a clear oil. The compound was deprotected using the previously described methods followed by HPLC purification to afford the desired product MIP-1097 as a whiter solid (270 grams, 90% yield). 1H NMR (400 MHz, DMSO-d6) δ 7.97 (d, 2H), 7.68 (t, 1H), 7.53 (d, 2H), 6.35 (dd, 2H), 4.10 (m, 1H), 4.00 (m, 1H), 2.65 (m, 2H), 2.22 (m, 2H), 1.9 (m, 1H), 1.7 (m, 1H), 1.55 (m, 1H), 1.45 (m, 1H), 1.35 (m, 2H), 1.25 (m, 2H), (3 CO2H not seen). ESMS m/z: 565 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08058449B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-515ddfb177e04b0bbea25fbf167f156e |
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| Source note | uspto-grants-2011_11 |
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