HuagongsheHuagongshe Chemistry Print Report · For research reference only
DL-Phenylalaninol → HCID 18610528, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | DL-Phenylalaninol | HCID 76652 | — |
| Reactant | HCID 18610529 | HCID 18610529 | — |
| Reactant | HCID 18610530 | HCID 18610530 | — |
| Product | HCID 18610528 | HCID 18610528 | — |
Reaction Steps
The procedure described in steps (a) to (h) of Example 1 was repeated, except that L-2-amino-3-phenyl-1-propanol was used as the starting material. Two isomers (derived from the asymmetric carbon atom to which the phenethyl group is attached), that is t-butyl α-{3(S)-benzyl-6(R)-[1(R)-ethoxycarbonyl-3-phenylpropylamino]-5-oxoperhydro-1,4-thiazepin-4-yl}acetate (isomer A) and t-butyl α-{3(S)-benzyl-6(R)-[1(S)-ethoxycarbonyl-3-phenylpropylamino]-5-oxoperhydro-1,4-thiazepin-4-yl}acetate (isomer B) were obtained as oils.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04699905 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-5e002efdff444940bf08e4d8950a0639 |
| Source note | uspto-grants-1987_10 |