HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → Benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(6-amino-1,3-benzothiazol-2-yl)benzamide | HCID 810331 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinazoline | HCID 2769364 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Benzamide | HCID 2331 | — |
Reaction Steps
N-[6-6,7-Dimethoxyquinazolin-4-ylamino)benzothiazol-2-yl]benzamide was prepared by heating a mixture of N-(6-aminobenzothiazol-2-yl)benzamide (IM 2, 30 mg, 0.111 mmol) and 4-chloro-6,7-dimethoxyquinazoline (Fluorochem, 25 mg, 0.111 mmol) in ethylene glycol (0.7 mL) to 100° C. for 2 h. Brine (25 mL) and saturated sodium hydrogencarbonate solution (25 mL) were added and the product was extracted with chloroform (3×40 mL). After drying out Na2SO4, the solvent was removed and the residue was purified by pTLC (petroleum ether:dichloromethane:methanol=12:14:3) to yield a yellow solid (19 mg, 41 μmol, 37%). LC/ESI-MS: m/z 458 [M+H]+; m/z=456 [M−H]−; Rt=2.88 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576090B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-51e3086cfc2f4f228c92f08fa9a17ca2 |
| Source note | uspto-grants-2009_08 |