HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Amino-4-pyrrol-1-yl-phenyl)-carbamic acid tert-butyl ester → 4-[3-(6-Methyl-pyridin-3-yl)-phenyl]-8-pyrrol-1-yl-1,3-dihydro-benzo[b][1,4]diazepin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Amino-4-pyrrol-1-yl-phenyl)-carbamic acid tert-butyl ester | HCID 69488996 | — |
| Reactant | 3-[3-(6-Methyl-pyridin-3-yl)-phenyl]-3-oxo-propionic acid tert-butyl ester | HCID 69489386 | — |
| Product | 4-[3-(6-Methyl-pyridin-3-yl)-phenyl]-8-pyrrol-1-yl-1,3-dihydro-benzo[b][1,4]diazepin-2-one | HCID 22317873 | — |
Reaction Steps
Compound 40 was prepared from (2-amino-4-pyrrol-1-yl-phenyl)-carbamic acid tert-butyl ester (J16) (273 mg, 1 mmol) and 3-[3-(6-methyl-pyridin-3-yl)-phenyl]-3-oxo-propionic acid tert-butyl ester (K3) (311 mg, 1 mmol) according to the general procedure M and subsequent treatment of the crude product according to the general procedure N. Obtained as a yellow solid (195 mg). MS (ISP) 393.2 [(M+H)+]; mp 213–214° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07235547B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-b1f3fc1b9ddc4615911554904b8c557b |
| Source note | uspto-grants-2007_06 |