HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethyl chloroformate → HCID 86634651, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethyl chloroformate | HCID 78528 | — |
| Reactant | HCID 69048547 | HCID 69048547 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 86634651 | HCID 86634651 | 89% |
Reaction Steps
To a solution of N-(2-mercaptobenzoyl)glycinamide (1.05 g, 5.0 mmol) in N,N-dimethylacetamide (DMA, 25 ml) was added 2-bromoethyl chloroformate (1.22 g, 6.5 mmol). The reaction mixture was stirred for 8 h, the solvent was evaporated to dryness, and the residue was triturated with ethyl ether (25 ml. The resulting precipitate was filtered, washed with water and dried over CaCO2, Yield: 89%. 1H NMR (DMSO-d6): 3.71 (t, 1H, CH2), 3.78 (d, 2H, CH2), 3.86 (t, 1H, CH2), 4.45 (t, 1H, CH2), 4.51 (t, 1H, CH2), 7.11 (brs, 1H, NH2), 7.30 (brs, 1H, NH2), 7.36-7.58 (m, 5H, Ar—H, NH2), 8.26 (t, 2H, Py-H), 8.36 (t, 1H, NH), 8.52 (t, 1H, NH), 8.66 (t, 1H, Py-H), 9.12 (d, 21, Py-H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076372B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-92ee909dfba74c68b61c4c329f77a7f6 |
| Source note | uspto-grants-2011_12 |