HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → Benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 10755041 | HCID 10755041 | — |
| Product | Benzamide | HCID 2331 | 110.1% |
Reaction Steps
The title compound was synthesized as in Example 37 using methyl sulfonyl chloride (0.8 g, 6.2 mmol) and 3-amino-N-(3,4-difluoro-phenyl)-4methoxy-benzamide (1.0 g, 3.6 mmol) to give 0.48 g of benzamide, N-(3,4-difluorophenyl)-4-methoxy-3-[[(methylamino) sulfonyl]amino]-. Microanalysis: C15H15F2N3O4S. 0.04 CH2Cl2.0.91H2O; calculated: C=46.18; H=4.35; N=10.74. found: C=46.18; H=4.36; N=10.64. MS: M++1=372 Da. 1HNMR (400 MHz, DMSO-d6) δ 10.26 (s, 1H), 8.60 (s, 1H), 7.93-7.88 (m, 2H), 7.74 (d, 8.4 Hz, 1H), 7.52-7.50 (m, 1H), 7.36 (q, J=9.4, 10.4 Hz, 1H), 7.13 (d, J=8.7 Hz, 2H), 3.88 (s, 3H), 2.49 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06906094B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-9634cd8739bd4979af73407bae5e5f68 |
| Source note | uspto-grants-2005_06 |