HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Methoxymethyl)cyclopropane-1-sulfonamide → 1-(Cyclopropylmethyl)cyclopropane-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Methoxymethyl)cyclopropane-1-sulfonamide | HCID 22499277 | — |
| Reactant | 1-Cyclopropylmethylcyclopropylsulfonylamine tert-butylcarbamate | HCID 22499312 | — |
| Product | 1-(Cyclopropylmethyl)cyclopropane-1-sulfonamide | HCID 22499285 | 65% |
Reaction Steps
This compound was obtained in 65% yield from 1-cyclopropylmethylcyclopropylsulfonylamine tert-butylcarbamate (from Step B.2.a) according to the procedure described for the synthesis of 1-methoxymethylcyclopropylsulfonamide (Step B.1.b). The compound was purified by column chromatography over SiO2 using 0% to 60% ethyl acetate in hexanes as the eluent: 1H NMR (CDCl3) δ 0.15 (m, 2H), 0.51 (m, 2H), 1.01 (m, 2H), 1.34 (m, 3H), 1.86 (d, J=7.0 Hz, 2H), 4.83 (s, 2H); 13C NMR (CDCl3) δ 4.65, 7.74, 11.26, 35.62, 41.21; LRMS m/z 193 (M++NH4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601686B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-990708acc33d4c8cbc28949b2b9a5e3c |
| Source note | uspto-grants-2009_10 |