HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 15698061, compound → HCID 178441674, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 15698061 | HCID 15698061 | — |
| Reactant | HCID 178509299 | HCID 178509299 | — |
| Product | HCID 178441674 | HCID 178441674 | — |
Reaction Steps
2-n-Butyl-1-[(2'-carboxybiphenyl-4-yl)methyl]-4-chloro-5-(methoxymethyl)imidazole (1.0 g) was first converted to the corresponding acid chloride and then coupled to 5-aminotetrazole by the procedure in Example 78, Part C to yield 0.87 g of a yellow glass. Flash chromatography in 100% ethyl acetate over silica gel yielded 77.1 mg of a white solid; m.p. 169°-173°. NMR (200 MHz, CDCl3, DMSO-d6) δ 12.0 (br s, 1H); 7.73-7.30 (m, 6H); 7.00 (d, 2H, J=7 Hz); 5.18 (s, 2H); 4.23 (s, 2H); 2.55 (t, 2H, J=7 Hz) 1.63 (t of t, 2H, J=7,7 Hz); 1.31 (t of q, 2H, J=7,7 Hz); 0.84 (t, 3H, J=7 Hz). Anal. Calcd. for C24H26ClN7O 2.(H2O)2 : C, 55.87; H, 5.86. Found: C, 56.01; H, 6.01.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05155118 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-71ae7126d12f4a3ca4b9ffb8accf293d |
| Source note | uspto-grants-1992_10 |