HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22852790, compound → HCID 10363941, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22852790 | HCID 22852790 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10363941 | HCID 10363941 | — |
Reaction Steps
A solution of dibenzyl N-(4-[N,N-bis-(2-chloroethyl)amino]-phenylcarbamoyl)-L-glutamate (1.138 g) in DMF (15 ml) was hydrogenated over 10% Pd/C for 16 h. After filtration and evaporation in vacuo, the residue was dissolved in CHCl3 (20 ml). After 18 h the crystalline precipitate was filtered off and dried in vacuo to obtain N-(4-[N,N-bis-(2-chloroethyl)amino]phenylcarbamoyl)-L-glutamic acid. Yield, 730 mg (93%). After recrystallization from acetone/CHCl3 microscopic rods formed m.p. 116°-118°. NMR (CD3 COCD3): δ8.0(s)1H; 7.2(d)2H; 6.6(d)2H; 6.2(d)2H NH; 4.4(m)1H; 3.6(m)8H; 2.5-1.9(m)4H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05714148 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-b869a0e551bf4e70bb73871f0eb45219 |
| Source note | uspto-grants-1998_02 |