HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 5-amino-2-bromobenzoate → N-[4-({7-[4-(TRIFLUOROMETHOXY)PHENYL]-1,2,3,4-TETRAHYDRONAPHTHALEN-1-YL}METHYL)BENZOYL]-beta-ALANINE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 5-amino-2-bromobenzoate | HCID 245495 | — |
| Reactant | Methyl 2-amino-5-bromobenzoate | HCID 736224 | — |
| Reactant | 2,5-Dibromobenzaldehyde | HCID 13540069 | — |
| Reactant | 4-Bromo-4'-(trifluoromethoxy)biphenyl-3-carbaldehyde | HCID 86621224 | — |
| Reactant | Tert-butyl N-(4-{2-[4-bromo-4-(trifluoromethoxy)biphenyl-3-yl]ethyl}benzoyl)-beta-alaninate | HCID 86761706 | — |
| Product | N-[4-({7-[4-(TRIFLUOROMETHOXY)PHENYL]-1,2,3,4-TETRAHYDRONAPHTHALEN-1-YL}METHYL)BENZOYL]-beta-ALANINE | HCID 11851838 | — |
Reaction Steps
The compounds in TABLE 1 were prepared using the chemistry described in EXAMPLES 1, 4, 5 and 6 or with following modifications: 1) EXAMPLES 47 to 50 (where R1=R21) were prepared as described in EXAMPLE 1 substituting 4-bromo-4′-(trifluoromethoxy)biphenyl-3-carbaldehyde with 2,5-dibromobenzaldehyde; 2) EXAMPLES 117 to 133 were prepared as described in EXAMPLE 1 substituting methyl 2-amino-5-bromobenzoate with methyl 5-amino-2-bromobenzoate; 3) EXAMPLES 111 to 113 were prepared from the intermediate from EXAMPLE 1 Step H using the procedure described in EXAMPLE 42A/42B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318760B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-efd1db6d98fb406784f43ff5b9d13ec2 |
| Source note | uspto-grants-2012_11 |