HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 4-(3-bromobenzene-1-sulfonyl)piperazine-1-carboxylate → HCID 59244286, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 4-(3-bromobenzene-1-sulfonyl)piperazine-1-carboxylate | HCID 45588490 | — |
| Reactant | HCID 67385372 | HCID 67385372 | — |
| Product | HCID 59244286 | HCID 59244286 | 33% |
Reaction Steps
From 4-(3-bromo-benzenesulfonyl)-piperazine-1-carboxylic acid tert-butyl ester (prepared from 3-bromobenzenesulfonyl chloride and piperazine-1-carboxylic acid tert-butyl ester, 83 mg) instead of 1-(3-bromo-benzenesulfonyl)-4-ethyl-piperazine in Example 1-D-96, a crude product of 4-[3-(4-{2-[bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidin-7-yl)-benzenesulfonyl]-piperazine-1-carboxylic acid tert-butyl ester was obtained, and then the PMB groups and BOC group were removed according to the above Deprotection method 1, to obtain the desired compound (D-132) as a yellow powder (32 mg, 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022205B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-04a6efaf361c479d97e3060254b8b21a |
| Source note | uspto-grants-2011_09 |