HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(6-Aminohexyl)-1-naphthalenesulfonamide → Naphthalene-1-sulfonic acid [6-(4-amino-quinazolin-2-ylamino)-hexyl]-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(6-Aminohexyl)-1-naphthalenesulfonamide | HCID 4314 | — |
| Reactant | 2-Chloroquinazolin-4-amine | HCID 252879 | — |
| Solvent | Isoamyl Alcohol | HCID 31260 | — |
| Product | Naphthalene-1-sulfonic acid [6-(4-amino-quinazolin-2-ylamino)-hexyl]-amide | HCID 9955360 | — |
Reaction Steps
A solution of naphthalene-1-sulfonic acid (6-amino-hexyl)-amide (0.450 g) and 2-chloro-quinazolin-4-ylamine (see: U.S. Pat. No. 3,956,495) (0.264 g) in 20 ml of isopentylalcohol is heated up to 120° C. for 15 h. Concentration of the reaction mixture followed by chromatography on silica gel (B1) yields naphthalene-1-sulfonic acid [6-(4-amino-quinazolin-2-ylamino)-hexyl]-amide as a white powder, melting at 98-101° C. Rf(B1) 0.28, FAB-MS: (M+H)+=450. Analytical C26H29N5O2S+HCl+H2O+0.6 1,4 dioxane. m.p. 98-101° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06713265B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-2b58371640ca4e1ca8f9e087a7656654 |
| Source note | uspto-grants-2004_03 |