HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578577Generated: October 30, 2026
Sulfuryl chloride → HCID 49781658, compound
https://huagongshe.com/reaction/578577
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| Reactant | 1-methyl-1H-imidazole-4-sulfonyl chloride | HCID 2736887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 49781658 | HCID 49781658 | 95% |
Reaction Steps
Mono-N-Boc-ethylenediamine (5; 5 g, 31.2 mmol, 1 eq) was sulfonylated with 1-methyl-1H-imidazole-4-sulfonyl chloride (6.76 g, 37.4 mmol, 1.2 eq). The appropriate sulfonyl chloride (1.2 equiv) was added to a solution of the amine (1 equiv) and DIPEA (2 equiv) in anhydrous CH3CN (0.1 M) at 0° C. The reaction was warmed to room temperature and stirred for 16 h, at which time the solvent was evaporated. The residue was re-dissolved in CH2Cl2, washed with 5% NaHCO3, water, brine, dried (Na2SO4), filtered and concentrated. After 16 h, the solvent was reduced and then the reaction mixture was dry-loaded onto silica gel and purified by flash column chromatography (eluent CH2Cl2/MeOH/NH4OH, 1092:7:1) to give the title compound as a white powder (9 g, 95%): δH (500 MHz, CD2Cl2) 1.37 (s, 9H, C(CH3)3), 2.99 (t, J=5.8 Hz, 2H, CH2NHSO2), 3.11 (q, J=5.8 Hz, 2H, CH2NHBoc), 3.71 (s, 3H, CH3), 5.53 (s, 1H, NHSO2), 5.68 (s, 1H, NHBoc), 7.48 (s, 1H, Im), 7.56 (s, 1H, Im); δC (125 MHz, CD2Cl2) 27.6, 33.5, 39.8, 42.6, 78.9, 124.0, 127.2, 139.2, 156.1; HRMS (ES+) calcd for [C11H20N4O4S+H] 305.1284. found 305.1294.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040563B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-8a14bc36396b48b8afdc9f7ebff5633e |
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| Source note | uspto-grants-2015_05 |
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