HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658340Generated: October 30, 2026
Methanesulfonyl chloride → HCID 86619833, compound
https://huagongshe.com/reaction/658340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (1R)-1-[5-(1,1-Dimethylethoxy)-2-(1-methylethoxy)-7-benzothiazolyl]-1,2-ethanediol | HCID 66745065 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86619833 | HCID 86619833 | — |
Reaction Steps
Methane sulfonylchloride (35 mg) is added to a solution of (R)-1-(5-tert-Butoxy-2-isopropoxy-benzothiazol-7-yl)-ethane-1,2-diol (100 mg) in pyridine (2 ml) at 0° C. The reaction mixture is then stirred at 0° C. for 3.5 hours. The solvent is removed in vacuo, The resulting residue is partitioned between HCl(aq) (2M) and ether. The organics is washed with water (1×), brine (1×), dried over MgSO4, filtered and the solvent removed in vacuo to give the title compound. 1H nmr (CDCl3, 400 MHz); 7.20 (d, 1H), 6.80 (d, 1H), 5.30 (sept, 1H), 5.10 (t, 1H), 4.30 (d, 2H), 3.00 (s, 3H), 1.40 (d, 6H), 1.30 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076489B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-25bfdf521a264a1696b57b19083b11dc |
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| Source note | uspto-grants-2011_12 |
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