HuagongsheHuagongshe Chemistry Print Report · For research reference only
2H-3,1-Benzoxazine-2,4(1H)-dione, 6-chloro-1-methyl- → 1-(2-Methylamino-5-chlorobenzoyl)-1H-indazol-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2H-3,1-Benzoxazine-2,4(1H)-dione, 6-chloro-1-methyl- | HCID 26724 | — |
| Reactant | Indazolinone | HCID 81829 | — |
| Product | 1-(2-Methylamino-5-chlorobenzoyl)-1H-indazol-3-ol | HCID 178482148 | 33.5% |
Reaction Steps
1H-Indazol-3-ol was reacted with N-methyl-5-chloroisatoic anhydride according to the general procedure A above and afforded the desired amine as a yellow solid in 33.5% yield; m.p. 210°-213° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04537966 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-8fe2ed2019f7483aa6fa2ac88f9e5b10 |
| Source note | uspto-grants-1985_08 |