HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Formyl-L-phenylalanine → (2S,3S,4R,5R)-5-(6-aminopurin-9-yl)-3-[[(2S)-2-formamido-3-phenyl-propanoyl]amino]-4-hydroxy-tetrahydrofuran-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Formyl-L-phenylalanine | HCID 759256 | — |
| Reactant | 1-(6-amino-9H-purin-9-yl)-1,3-dideoxy-3-amino-beta-D-ribofuranuronic acid monohydrate | HCID 70465522 | — |
| Product | (2S,3S,4R,5R)-5-(6-aminopurin-9-yl)-3-[[(2S)-2-formamido-3-phenyl-propanoyl]amino]-4-hydroxy-tetrahydrofuran-2-carboxylic acid | HCID 476106 | 27.1% |
Reaction Steps
1-(6-Amino-9H-purin-9-yl)-1,3-dideoxy-3-(N-formyl-L-phenylalanylamino)-β-D-ribofuranuronic acid (58 mg) was prepared by reacting 1-(6-amino-9H-purin-9-yl)-1,3-dideoxy-3-amino-β-D-ribofuranuronic acid monohydrate (140 mg) prepared in Example 99 with N-hydroxysuccinimide ester of N-formyl-L-phenylalanine (130 mg) according to a similar manner to that of Example 5, mp. 169°-181° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04479942 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-ea64af9a316f42ea8c11911fd6d7df00 |
| Source note | uspto-grants-1984_10 |